CLASS II ONGOING Device recall · Reported 8 Apr 2026 · FDA Enforcement Report
Medline Anterior Hip Pack Dynj64672b recalled by Medline Industries
Medline Industries is recalling Medline Anterior Hip Pack Dynj64672b, distributed nationwide in the US. The recall was initiated on 16 Feb 2026 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1711-2026
- FDA event ID
- 98530
- Recalling firm
- Medline Industries, Northfield, IL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 16 Feb 2026
- FDA classified
- 1 Apr 2026
- Reported
- 8 Apr 2026
- Type
- Voluntary: Firm initiated
- Reason category
- Foreign Material
- Device type
- Hip & Knee Implants
Timeline
| 16 Feb 2026 | Recall initiated by company | |
| 1 Apr 2026 | Classified by FDA | +44 days |
| 8 Apr 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
MEDLINE ANTERIOR HIP PACK DYNJ64672B
Where it was distributed
US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.
Nationwide CaliforniaFloridaIllinoisIndianaKentuckyMassachusettsMarylandMontanaNew YorkOhioPennsylvaniaTennesseeTexas
Questions about this recall
Why was it recalled?
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
Which lots are affected?
UDI-DI 10195327377496 (EA) 40195327377497 (CS) LOT 23LMD300
Where was it sold?
US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
6 other products · FDA event 98530This product is part of a recall event; the main page for the event is Thoracic Robots, Dynj908777b recalled by Medline Industries.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Thoracic Robots, Dynj908777b recalled by Medline Industries | Medline Industries | Foreign Material | Nationwide | |
| CLASS II | Airway Exam Kit, DYKE1796 recalled by Medline Industries | Medline Industries | Foreign Material | Nationwide | |
| CLASS II | Medline kits containing Olympus biopsy valves: Bronchoscopy recalled | Medline Industries | Foreign Material | Nationwide | |
| CLASS II | Medline kits containing Olympus biopsy valves recalled | Medline Industries | Foreign Material | Nationwide | |
| CLASS II | Medline convenience kits containing Olympus biopsy valves recalled | Medline Industries | Foreign Material | Nationwide | |
| CLASS II | Medline kits containing Olympus biopsy valves: BAL KIT recalled | Medline Industries | Foreign Material | Nationwide |
More recalls from Medline Industries
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|---|---|---|---|---|---|
| Device | CLASS II | Medline Drape C-section W/Pouch ST 7/CS, Medline Product Number recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as: Fetal Surgery Cds-lf recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Drape C-section Fen Clr Screen W, Medline Product Number recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as: C-section Pack recalled | Medline Industries | Other | Nationwide |
Other Hip & Knee Implants recalls
All 3,118| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Halyard Anterior Hip Pack recalled by Avid Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS II | Halyard Anterior Hip Pack recalled by Avid Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as: Hip Scope Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | TS Femoral Prep Tray, Triathlon recalled by Howmedica Osteonics | Howmedica Osteonics | Sterility | NJ |
| Device | CLASS II | Grafton" DBM and Grafton Plus" DBM contain demineralized recalled | Medtronic Sofamor Danek USA | Other Bacterial Contamination | Nationwide |