Recalls in Minnesota
56,290 recalls cover Minnesota, counting both recalls distributed specifically to the state and nationwide recalls. The latest was reported on 9 Oct 2026. 14,117 are ongoing right now.
Total recalls 56,290 since 2012
Last 12 months 3,999 reported
Class I 9,206 16% of total
Ongoing 14,117 latest 9 Oct 2026
Recalls per month, last 24 months click a bar for that month
Severity split
Class I 9,206 16% Class II 44,295 79% Class III 2,773 5% Other/pending 16
Why products are recalled By year 2026 3,0935% 2025 3,2366% 2024 3,7887% 2023 3,6036% 2022 3,8527% 2021 2,8515% 2020 3,6056% 2019 4,3308% 2018 4,3048% 2017 4,2027%
Ongoing recalls in Minnesota 14,117 active
All recalls in minnesota, newest first 56,290 total
Reported Class Recall Company Reason Where 9 Oct 2026 Drug ANNOUNCED Par Pharmaceutical Brevital Sodium 500 mg/vial for Injection recalled Par Pharmaceutical Par Health Particulate Matter Nationwide 8 Oct 2026 Food ANNOUNCED Broccoli Sprouting Seeds recalled by Gardeners Basics Gardeners Basics Gardeners Basics Salmonella Nationwide 7 Oct 2026 Food CLASS I Alfalfa Sprouting Seeds recalled by Todd's Seeds Alfalfa Sprouting Todd's Seeds Salmonella Nationwide 7 Oct 2026 Food CLASS I Sprouting Seed Mix - Broccoli, Radish, Alfalfa recalled by Todd's Seeds Sprouting Todd's Seeds Salmonella Nationwide 7 Oct 2026 Food CLASS I Alfalfa & Mung Bundle each), packaged separately recalled Alfalfa Todd's Seeds Salmonella Nationwide 7 Oct 2026 Food CLASS I Variety Pack of Sprouting Seeds - Broccoli, Alfalfa recalled Variety Todd's Seeds Salmonella Nationwide 7 Oct 2026 Food CLASS I Broccoli & Friends Sprouting Seed Mix - Broccoli, Alfalfa recalled Broccoli Todd's Seeds Salmonella Nationwide 7 Oct 2026 Food CLASS I Salad Sprouting Mixture - Broccoli, Mustard, Alfalfa and Cabbage recalled Todd's Seeds Salmonella Nationwide 7 Oct 2026 Device CLASS II SmartPath to dStream for XR and 3.0T recalled by Philips North America Philips North America Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Hopkins Telescope 30¿ recalled by Karl Storz Endoscopy Karl Storz Endoscopy Packaging Defects Nationwide 7 Oct 2026 Device CLASS II Disposable Tourniquet Cuff, 24" X 4" 1-Line, Yellow recalled ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Mpr Single Use Tourniquet Cuff 15" 1 Line recalled by ASP Global ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 1-Line (CS Plum recalled ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II NOxBOXi Nitric Oxide Delivery System recalled Noxbox Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Palacos R pro recalled by Heraeus Medical GmbH (Dental Heraeus Medical GmbH (Dental Division) Packaging Defects Nationwide 7 Oct 2026 Device CLASS II Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065 recalled Percussionaire Other Nationwide 7 Oct 2026 Device CLASS II Disposable Tourniquet Cuff, 44" X 4" 2-Line, Green recalled ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Expressaire Disposable Tourniquet Cuff, 44" X 4" 2-Line (CS Green recalled ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Fisher Scientific Sure-Vue Urine hCG Strip recalled by Alere San Diego Alere San Diego Potency & Assay Nationwide 7 Oct 2026 Device CLASS II Mpr Single Use Tourniquet Cuff 24" 2 Line recalled by ASP Global ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Expressaire Disposable Tourniquet Cuff, 34" X 4" 1-Line (CS Blue recalled ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Expressaire Disposable Tourniquet Cuff, 24" X 4" 2-Line (CS Yellow recalled ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Positron Emission Tomography and Computed Tomography System recalled Shanghai United Imaging Healthcare Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Mpr Single Use Tourniquet Cuff 34" 2 Line recalled by ASP Global ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 2-Line (CS Plum recalled ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Disposable Tourniquet Cuff, 44" X 4" 1-Line, Green recalled ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Upgrade to MR recalled by Philips North America Philips North America Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Mpr Disposable Tourniquet Cuff 18" 2 Line recalled by ASP Global ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Disposable Tourniquet Cuff, 24" X 4" 2-Line, Yellow recalled ASP Global Device Malfunction Nationwide 7 Oct 2026 Device CLASS II Expressaire Disposable Tourniquet Cuff, 18" X 4" 1-Line (CS Red recalled ASP Global Device Malfunction Nationwide
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About recalls in Minnesota
This list combines recalls whose distribution names Minnesota with nationwide recalls. Products distributed to a few states can still reach others through secondary distribution, so check lot codes rather than assuming.