| Food | CLASS I | Meat and Poultry Products recalled by Kayem Foods | Kayem Foods | Temperature Abuse | |
| Food | ANNOUNCED | Gelatelli Coffee & Vanilla Gelato with Coffee Sauce & Cookie Pieces recalledGelatelli | Lidl US | Listeria | 10 states |
| Food | ANNOUNCED | Family Farmstead Raw Mild Cheddar Cheese recalledFamily Farmstead | Family Farmstead Dairy | E. coli | |
| Food | ANNOUNCED | Family Farmstead Raw Mild Cheddar Cheese recalledFamily Farmstead | Family Farmstead Dairy | E. coli | NJ, NY |
| Food | CLASS II | Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC recalledElevated Edibles | Sweet Sensi | Other Bacterial Contamination | Nationwide |
| Food | CLASS II | Gatorade Lemon Lime Zero, and Gatorade Orange Zero recalled by PepsicoGatorade | Pepsico | Undeclared Allergens | 37 states |
| Food | CLASS II | Frozen Mushroom & Onion Pizza recalled by Saint Francis Apizza | Saint Francis Apizza | Undeclared Soy | KY, OH |
| Food | CLASS I | Leasa Living Alfalfa Sprouts recalled by Leasa IndustriesLeasa Living | Leasa Industries | E. coli | FL, NH |
| Food | CLASS II | Lemon Blueberry Loaf recalled by J K Patisserie & Bakery | J K Patisserie & Bakery | Undeclared Soy | NJ, NY |
| Food | CLASS I | biQ-FEL recalled by A&P Creations | A&P Creations | Undeclared Allergens | Nationwide |
| Food | CLASS II | Frozen Supreme Pizza recalled by Saint Francis Apizza | Saint Francis Apizza | Undeclared Soy | KY, OH |
| Food | CLASS I | Donutful Chocolate Dipped Vanilla Cake Donuts -/Case recalledDonutful | The Better Bakehouse Snack | Undeclared Milk | Nationwide |
| Food | CLASS I | Lemon Alfredo Fettuccine recalled by Gias Food | Gias Food | Listeria | Nationwide |
| Food | CLASS II | Frozen Cheese Pizza recalled by Saint Francis Apizza | Saint Francis Apizza | Undeclared Soy | KY, OH |
| Food | CLASS II | Croissant; packaged in cardboard box; Ingredients recalledCroissant | J K Patisserie & Bakery | Undeclared Egg | NJ, NY |
| Food | CLASS I | Leasa Alfalfa Sprouts recalled by Leasa IndustriesLeasa Alfalfa | Leasa Industries | E. coli | FL, NH |
| Food | CLASS II | Chocolate Chip Cookies recalled by J K Patisserie & Bakery | J K Patisserie & Bakery | Undeclared Soy | NJ, NY |
| Food | CLASS II | Pastel de Queso (Cheese Pie) recalled by Queso Palmita GPPastel | Queso Palmita GP | Undeclared Milk | TX |
| Device | CLASS II | Plastics Tray kits recalled by Avid Medical | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS III | Passport Series Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Heart Prep Tray kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Pack Open Heart Cfh kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | TufTex¿ Over-the-Wire Embolectomy Catheter recalled | LeMaitre Vascular | Other | Nationwide |
| Device | CLASS III | T1 Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Sperm Ab Elisa (96 well plate test) recalled by DRG International | DRG International | Other | Nationwide |
| Device | CLASS II | Intellijoint Navigation System: Workstation G2 Configured recalled | Intellijoint Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Adaptable Beach Chair Beach Chair surgical patient positioner recalled | Quantum OPS | Device Malfunction | Nationwide |
| Device | CLASS II | Laparoscopic Prostatectomy kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | BeneView Series recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS III | cPM Series Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | DxC 500 AU Clinical Chemistry Analyzers: AU w/out ISE recalled | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Alphenix Infx-8000C/B5 recalled by Canon Medical System USA | Canon Medical System USA | Other | Nationwide |
| Device | CLASS II | Halyard Laparoscopy Comprehensive Pack II recalled | GRI Medical & Electronic Technology | Other | Nationwide |
| Device | CLASS II | Endovascular Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | BeneVision Series Telemetry Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Davinci LAP/GYN kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Sediplast; Model/Catalog Numbers recalled by Polymedco, Inc. / Polymedco | Polymedco, Inc. / Polymedco Cancer Diagnostic Products | Other | Nationwide |
| Device | CLASS II | DxC 500i Clinical Analyzer Modules: DxC 500 AU Module w/ISE recalled | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Packs containing Medtronic Microstream Components recalled | Cardinal Health 200 | Device Malfunction | IL |
| Device | CLASS III | Panorama and Telemetry Monitoring System recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Major Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | Kit: Urinary Clean Catch 20/cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Device Malfunction | CA |
| Device | CLASS II | Gyn Laparoscopy/Laparotomy kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | BeneVision N1 and N-Series Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | ABD Hysterectomy kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Gyn Laparoscopy Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Rollator, Bariatric, Basic Steel, Burgundy recalled | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Verify Biological Steam Test Pack recalled by Steris | Steris | Sterility | Nationwide |
| Device | CLASS II | Davinci Trucustom Bundle kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | ePM Series Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Urology Major kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | HexaVue Focus Integration System, a single recalled by Steris | Steris | Device Malfunction | Nationwide |
| Device | CLASS II | Craniotomy Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | My3D Personalized Pelvic Implant, Porous, Left recalled | Onkos Surgical | Other | Nationwide |
| Device | CLASS II | Adult Heart Tray Shands Jacks kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Verify Biological/Integrator Challenge Pack recalled by Steris | Steris | Sterility | Nationwide |
| Device | CLASS II | Robotic Prostatectomy Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Verify Dual Species Self-Contained Biological Indicator recalled | Steris | Sterility | Nationwide |
| Device | CLASS II | Glypto Device, Glypto Cryo Machine recalled by Limitless Cryo | Limitless Cryo | Other | Nationwide |
| Device | CLASS II | Verify Dual Species Self-Contained Biological Indicator recalled | Steris | Sterility | Nationwide |
| Device | CLASS II | Verify Biological/Integrator Challenge Pack recalled by Steris | Steris | Sterility | Nationwide |
| Device | CLASS II | Battle Bandage recalled by Safeguard US Operating | Safeguard US Operating | Foreign Material | Nationwide |
| Device | CLASS II | Nihon Kohden CNS-6200 Series Central Nurse Station recalled | Nihon Kohden America | Device Malfunction | Nationwide |
| Device | CLASS II | My3D Personalized Pelvic Implant, Porous, Left recalled | Onkos Surgical | Other | Nationwide |
| Device | CLASS II | Rollator, Bariatric, Basic Steel, Blue recalled by Medline Industries | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Spectral CT and Spectral CT 7500 RT recalled by Philips Medical Systems | Philips Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | MiniMed Flex Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Labeling Errors | Nationwide |
| Device | CLASS II | Verify Biological Steam Test Pack recalled by Steris | Steris | Sterility | Nationwide |
| Device | CLASS II | Bard Ep Xt Decapolar Steerable, Diagnostic Ep Catheter, 6f recalled | Stryker Sustainability Solutions | Particulate Matter | Nationwide |
| Drug | CLASS II | Apothecary NAD+ Injection 200 mg/mL Sterile Multi-Dose Vial recalled | Apothecary Pharma | Sterility | Nationwide |
| Drug | CLASS II | Sterile Eye Drops Redness Relief (Glycerin recalledLeader Eye Drops Redness Relief | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Sermorelin Acetate 1 MG/ML Injectable recalled by Carolina Infusion | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Semaglutide 3 MG/ML Injectable, . syringes recalled by Carolina Infusion | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Semaglutide/cyanocobalamin 3/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Sterile EYE Drops AC (tetrahydrozoline HCl recalledGoodsense Eye Drops Irritation Relief | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS III | Tretinoin Cream USP, 0.05% tube recalledTretinoin | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Semaglutide/cyanocobalamin 9/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Artificial Tears Sterile Lubricant Eye Drops recalledLeader Artificial Tears 15 Ml | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Tirzepatide 26 MG/ML Injectable recalled by Carolina Infusion | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Tris/Tromethamine, USP, GMP, API Grade recalled by BioSpectra | BioSpectra | Potency & Assay | CA |
| Drug | CLASS II | Tirzepatide/cyanocobalamin 76/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Eye Drops Maximum, Redness Relief, Sterile recalledTarget Eye Drops Maximum Redness Relief Eye | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS III | Tretinoin Cream UPS recalled by SUN Pharmaceutical IndustriesTretinoin | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Tirzepatide/cyanocobalamin 64/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Sterile High Performance Ultra Lubricating Eye Drops recalledLeader Ultra Lubricating Eye Drops | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Tirzepatide/cyanocobalamin 85/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS III | Tretinoin Cream USP, 0.05% tube recalledTretinoin | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/2/20, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Lidocaine Ointment USP, 5% (Generic for Xylocaine) recalled | Preferred Pharmaceuticals | Packaging Defects | Nationwide |
| Drug | CLASS II | Tirzepatide Injection, 18mg/mL Sterile Multi-Dose Vial recalled | Apothecary Pharma | Sterility | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros), 30/1/40, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Sterile Eye Drops, Original recalled by K.C. PharmaceuticalsGoodsense Eye Drops Original Formula | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Imaavy (nipocalimab-aahu) Injection, 300 mg recalledImaavy | J&J Innovative Medicine | Particulate Matter | OH |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/2/40 recalled by Carolina Infusion | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Fosfomycin Tromethamine Granules for Oral Solution recalled by Cipla USAFosfomycin Tromethamine | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Sterile EYE Drops Advanced Relief, (dextran recalledLeader Advanced Relief Eye Drops | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/1/60, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/1/10, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/1/20, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Tirzepatide/cyanocobalamin 26/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Quad-mix( Papav/phento/alpros/trop) Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Sterile Lubricant Dry Eye Relief Eye Drops recalledLeader Dry Eye Relief Eye Drops | K.C. Pharmaceuticals | Sterility | Nationwide |
| Food | ANNOUNCED | Para Bien Al Grano recalled by Pan PepinPara Bien | Pan Pepin | Undeclared Sesame | PR |
| Drug | ANNOUNCED | Par Health and Endo USA Argatroban Injection 250 mg/ (100 mg/mL) recalledPar Health and Endo USA | Par Health USA | Particulate Matter | Nationwide |
| Food | CLASS II | Frozen Pepperoni Pizza recalled by Saint Francis Apizza | Saint Francis Apizza | Undeclared Soy | KY, OH |
| Food | CLASS II | Salsa Bean Dip Express Tray recalled by WinCo Foods | WinCo Foods | Foreign Material | 8 states |
| Food | CLASS II | Mezzetta Golden Greek Peperoncini Medium Heat G.L. Mezzetta recalledMezzetta | G L Mezzetta | Foreign Material | 22 states |
| Food | CLASS I | Alfalfa Sprouting Seeds recalled by Berlin SeedsAlfalfa Sprouting | Berlin Seeds | Salmonella | Nationwide |
| Food | CLASS II | Cranberry Chicken Salad Wedge package in Wedge recalledCranberry | Freshpoint Central Florida | Undeclared Allergens | FL, GA |
| Food | CLASS I | X10 Natural Enhancement Supplement, 7 sachets/box recalled | A&P Creations | Undeclared Allergens | Nationwide |
| Food | NOT YET CLASSIFIED | Graziers Raw Milk Sharp Cheddar recalled by Sierra Nevada CheeseGraziers | Sierra Nevada Cheese | E. coli | 13 states |
| Food | ANNOUNCED | Pan Pepín Inc. Emite Alerta por Alérgenos en el Producto recalled | | Other | |
| Food | ANNOUNCED | Starfish Seafood Cold Smoked Salmon recalled by Krasnyi OktyabrStarfish Seafood | Krasnyi Oktyabr | Listeria | 6 states |
| Food | ANNOUNCED | Starfish Seafood Cold Smoked Salmon, Halibut, and Trout recalledStarfish Seafood | Krasnyi Oktyabr | Listeria | 6 states |
| Food | ANNOUNCED | Riad's Oliva to Go Baba Ghanouj, Spicy Baba Ghanouj, and Hummus recalledRiad's Oliva to Go | Oliva | Undeclared Sesame | CT, MA |
| Drug | ANNOUNCED | Par Pharmaceutical Brevital Sodium 500 mg/vial for Injection recalledPar Pharmaceutical | Par Health | Particulate Matter | Nationwide |
| Food | ANNOUNCED | Broccoli Sprouting Seeds recalled by Gardeners BasicsGardeners Basics | Gardeners Basics | Salmonella | Nationwide |
| Food | CLASS I | Alfalfa Sprouting Seeds recalled by Todd's SeedsAlfalfa Sprouting | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS II | Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen recalledOrganiccs Absolutely | Pacific Health Sciences | Undeclared Fish & Shellfish | 6 states |
| Food | CLASS II | Cloud Cafe branded Collagen Milk recalled by TojiCloud Cafe | Toji | Undeclared Allergens | CA |
| Food | CLASS I | Sprouting Seed Mix - Broccoli, Radish, Alfalfa recalled by Todd's SeedsSprouting | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS II | Khazana The Treasure Spice Magic Fennel Candy recalled by SLT FoodsKhazana | SLT Foods | Undeclared Allergens | NY |
| Food | CLASS I | Alfalfa & Mung Bundle each), packaged separately recalledAlfalfa | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS I | Variety Pack of Sprouting Seeds - Broccoli, Alfalfa recalledVariety | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS I | Salata Salad Kitchen Jalapen¿o Avocado Dressing recalledSalata | Salata Dressings | Salmonella | GA, NC, TX |
| Food | CLASS I | Coco G's Courmet Flaming Cheddar Hots, Spicy Cheddar Cheese Popcorn recalledCoco G's | Coco G's Snack Foods | Salmonella | IL, WI |
| Food | CLASS I | Broccoli & Friends Sprouting Seed Mix - Broccoli, Alfalfa recalledBroccoli | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS II | 7up Tropical beverage, shelf stable can in a wrap recalled | Admiral Beverage | Undeclared Allergens | UT |
| Food | CLASS I | Salad Sprouting Mixture - Broccoli, Mustard, Alfalfa and Cabbage recalled | Todd's Seeds | Salmonella | Nationwide |
| Device | CLASS II | SmartPath to dStream for XR and 3.0T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Hopkins Telescope 30¿ recalled by Karl Storz Endoscopy | Karl Storz Endoscopy | Packaging Defects | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 24" X 4" 1-Line, Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 15" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 1-Line (CS Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | NOxBOXi Nitric Oxide Delivery System recalled | Noxbox | Device Malfunction | Nationwide |
| Device | CLASS II | Palacos R pro recalled by Heraeus Medical GmbH (Dental | Heraeus Medical GmbH (Dental Division) | Packaging Defects | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065 recalled | Percussionaire | Other | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 44" X 4" 2-Line, Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 44" X 4" 2-Line (CS Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Fisher Scientific Sure-Vue Urine hCG Strip recalled by Alere San Diego | Alere San Diego | Potency & Assay | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 24" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 34" X 4" 1-Line (CS Blue recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 24" X 4" 2-Line (CS Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 34" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 2-Line (CS Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 44" X 4" 1-Line, Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Upgrade to MR recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Disposable Tourniquet Cuff 18" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 24" X 4" 2-Line, Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 18" X 4" 1-Line (CS Red recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 34" X 4" 2-Line (CS Blue recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV-1C recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Opportunity Pro recalled by American Nitrile Operations | American Nitrile Operations | Device Malfunction | Nationwide |
| Device | CLASS II | Atellica CH Revised C-Reactive Protein (RCRP) recalled | Siemens Healthcare Diagnostics | Other | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 24" X 4" 2-Line (CS Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 8" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Palacos R+G pro recalled by Heraeus Medical GmbH (Dental | Heraeus Medical GmbH (Dental Division) | Packaging Defects | Nationwide |
| Device | CLASS II | Palacos MV pro recalled by Heraeus Medical GmbH (Dental | Heraeus Medical GmbH (Dental Division) | Packaging Defects | Nationwide |
| Device | CLASS II | Medical convenience kits containing BD CliniClean Pericare recalled | American Contract Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Tandem t:slim mobile application t:slim Mobile Application, iOS recalled | Tandem Diabetes Care | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 24" X 4" 1-Line (CS Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Packs Containing Stryker StrykeFlow PS recalled | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | McKesson Consult hCG Urine Cassette recalled by Alere San Diego | Alere San Diego | Potency & Assay | Nationwide |
| Device | CLASS II | Travel Air, Product Number: S00055 recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Systems/units containing affected recalled | Beckman Coulter Mishima K.K | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 34" X 4" 2-Line, Blue recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 30" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 12" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Opportunity Flex recalled by American Nitrile Operations | American Nitrile Operations | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus M3 Gold Autoclavable Lateral Telescope recalled | Olympus Corporation of the Americas | Sterility | PA |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 26" X 6" 1-Line (CS Orange recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 30" X 4" 2-Line (CS White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 34" X 4" 1-Line (CS Blue recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 30" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Elition S and Ingenia Elition recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 8" X 2.5" 2-Line (CS recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Tripp-Lite P580-025 25ft DisplayPort Cable recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 44" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 15" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Charlotte Claw Screw recalled by Wright Medical Technology | Wright Medical Technology | Other | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 30" X 4" 2-Line, White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Packs Containing Stryker StrykeFlow PS recalled | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 18" X 4" 1-Line, Red recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 8" X 2.5" 1-Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Ambition S and Ingenia Ambition recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 2-Line (CS Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 15" X 4" 1-Line (CS Gray recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 15" X 4" 2-Line (CS Gray recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Blue Seal SE and Blue Seal XE recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Palacos MV+G pro recalled by Heraeus Medical GmbH (Dental | Heraeus Medical GmbH (Dental Division) | Packaging Defects | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 34" X 4" 2-Line (CS Blue recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Fisher Scientific Sure-Vue Urine hCG recalled by Alere San Diego | Alere San Diego | Potency & Assay | Nationwide |
| Device | CLASS II | SmartPath to MR recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | MR 5300; Model number (REF): 1. 782110, 2. 782152 recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 24" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 44" X 4" 1-Line (CS Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Medical convenience kits containing BD CliniClean Pericare recalled | American Contract Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Disposable Tourniquet Cuff 20" Dual Bladder, 1 Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | EnCor EnCompass Breast Biopsy and Tissue Removal System Console recalled | Bard Peripheral Vascular | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 34" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 44" X 4" 2-Line (CS Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Disposable Tourniquet Cuff 20" Dual Bladder, 2 Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Pipeline Flex Embolization Device with Shield Technology recalled | Micro Therapeutics | Labeling Errors | Nationwide |
| Device | CLASS II | Olympus M3 Gold Autoclavable Foroblique Telescope recalled | Olympus Corporation of the Americas | Sterility | PA |
| Device | CLASS II | Impulsator, Product Number: S00010, Phasitron recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 12" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 15" X 4" 2-Line (CS Gray recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 30" X 4" 1-Line, White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | NovaSeq 6000Dx including Dragen Server recalled by Illumina | Illumina | Potency & Assay | Nationwide |
| Device | CLASS II | Expressaire Disposable BB Tournquet Cuff recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | In-Line Valve, Product Number: P5-TEE recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 18" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 18" X 4" 1-Line (CS Red recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 26" Dual Bladder, 2 Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Upgrade dStream recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS I | VentStar Resus Neo recalled by Draeger | Draeger | Packaging Defects | Nationwide |
| Device | CLASS II | Fisher Scientific Sure-Vue Serum/Urine hCG recalled by Alere San Diego | Alere San Diego | Potency & Assay | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 44" X 4" 1-Line (CS Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Philips Medical Systems Technologies Ltd recalled | Philips North America | Device Malfunction | MA |
| Device | CLASS II | Disposable Tourniquet Cuff, 18" X 4" 2-Line, Red recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 38" X 4" 1-Line (CS recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 18" X 4" 2-Line (CS Red recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Packs Containing Stryker StrykeFlow PS recalled | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | Evolution upgrade 1.5T amd Evolution upgrade 3.0T recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 34" X 4" 1-Line, Blue recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia 1.5T, 1.5T CX, and 1.5T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable BB Tournquet Cuff recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | System (RED 62 Reperfusion Catheter) recalled by Penumbra | Penumbra | Device Malfunction | Nationwide |
| Device | CLASS I | Medline Basic Homecare Beds and Medlite Homecare Beds recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Performance Pro recalled by American Nitrile Operations | American Nitrile Operations | Device Malfunction | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV-2C recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Ferndale Laboratories recalled by Custom Interventional Pain | Custom Interventional Pain Management | Foreign Material | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 24" X 4" 1-Line (CS Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Philips IntraSight Plus recalled by Volcano | Volcano | Device Malfunction | Nationwide |
| Device | CLASS II | Medical convenience kits containing BD CliniClean Pericare recalled | American Contract Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 30" X 4" 1-Line (CS White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 12" X 3.5" 2-Line, Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 18" X 4" 2-Line (CS Red recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 30" X 4" 1-Line (CS White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum PureFlow Standard Heat Exchanger High Flow 3/8 recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Presource Packs Containing Stryker StrykeFlow PS recalled | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 20" X 6" 1-Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | MR 7700; Model number (REF): 1. 782120, 2. 782153 recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 44" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV HC recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Embosphere 500-700 micrometer Syringe Sterile Steam recalled | Merit Medical Systems | Sterility | Nationwide |
| Device | CLASS II | Quantum PureFlow Standard Heat Exchanger High Flow 3/8 recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Expressaire Disposable BB Tournquet Cuff recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 8" X 2.5" 2-Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia 3.0T and 3.0T CX recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS I | Medline Basic Homecare Beds and Medlite Homecare Beds recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 30" X 4" 2-Line (CS White recalled | ASP Global | Device Malfunction | Nationwide |
| Drug | CLASS II | Ranolazine Extended-Release Tablets, 1000 mg recalledRanolazine | Ajanta Pharma USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Buprenorphine Hydrochloride, Injection 0.3 mg/mL recalledBuprenorphine Hydrochloride | Par Health USA | Other | Nationwide |
| Drug | CLASS II | Benzoyl Peroxide Wash recalled by SV Labs Toronto | SV Labs Toronto | Sterility | IL |
| Drug | CLASS II | Paroxetine Extended-Release Tablets, 37.5mg recalled by ApotexParoxetine Hydrochloride | Apotex | Potency & Assay | Nationwide |
| Drug | CLASS II | Zoladex (goserelin) implant, 3.6 mg, One single-Use Syringe recalledZoladex | TerSera Therapeutics | Temperature Abuse | Nationwide |
| Drug | CLASS II | Focus PI Hypromellose 0.7% Formula, 0.3 FL O per vial, Sterile recalledFocus Pi | Aurolab Trust | Sterility | VA |
| Drug | CLASS II | Estradiol Gel, 0.1%, 0.25 mg, 30-packets recalledEstradiol | Amneal Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Benzoyl Peroxide Wash recalled by SV Labs Toronto | SV Labs Toronto | Sterility | IL |
| Food | ANNOUNCED | Broccoli Seeds - Calabrese recalled by Eden BrothersEDEN BROTHERS | Eden Brothers | Salmonella | Nationwide |
| Food | ANNOUNCED | Babies' Magic Tea Baby Sleep Gripe Water recalledBabies' Magic Tea | Pacific Health Sciences | Undeclared Allergens | |
| Food | ANNOUNCED | Rapture Preworkout Dietary Supplement Powder recalled by Leader FormulasRAPTURE | Leader Formulas | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Lior Cinnamon Ground Seasoning recalled by Galil ImportingLior Cinnamon | Galil Importing | Lead & Heavy Metals | 6 states |
| Food | CLASS II | Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil recalledKofinas Garlic | Lmsi | Hidden Drug Ingredients | 13 states |
| Food | HEALTH ALERT | Ineligible Chicken Vienna-Style Sausage Products Illegally recalled | FSIS | Processing Deviation | |
| Device | ANNOUNCED | StatStrip Glucose Hospital Meter System recalled by Nova BiomedicalNova Biomedical StatStrip | Nova Biomedical | Device Malfunction | |
| Food | ANNOUNCED | Nature's Own Hawaiian Bread single loaf recalled by Flowers FoodsNature's Own | Flowers Foods | Undeclared Milk | 5 states |
| Food | CLASS I | Ineligible Pork Cracklings Products recalled by Inexport Logistics | Inexport Logistics | Processing Deviation | |
| Food | ANNOUNCED | Great Value, Trader Joe’s Organic Blueberries recalledGreat Value, Trader Joe’s | Frutas y Hortalizas del Sur | E. coli | 35 states |
| Food | ANNOUNCED | Home Grown Green Sprouting Calabrese Broccoli Seeds recalledHome Grown | EAK Distribution | Salmonella | Nationwide |
| Food | ANNOUNCED | Ice cream recalled by Stewart’s ShopStewart’s Shops | Stewart’s Shop | Foreign Material | NH, NY, VT |
| Drug | ANNOUNCED | Greewich Glutathione Injection recalled by Greenwich RxGreewich | Greenwich Rx | Packaging Defects | Nationwide |
| Food | ANNOUNCED | Bettergoods Pasta recalled by Gias FoodsBettergoods | Gias Foods | Listeria | Nationwide |