Folsom Metal Products, Inc.: Device Recall
Recall #Z-2581-2025 · 08/21/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2581-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Folsom Metal Products, Inc.
- Status
- Ongoing
- Date Initiated
- 08/21/2025
- Location
- Pelham, AL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 490 units
Reason for Recall
Labeling includes shelf life that has not been validated.
Product Description
Frontier Devices, REF: 301.916S1, 16 mm Distraction Pin, 10 single packs , Rx Only, Sterile
Distribution Pattern
US Nationwide distribution in the states of AL, CA, FL, GA, IL, MD, MI, PA, TX.
Other Recalls by Folsom Metal Products, Inc.
- Class II: Risk 08/21/2025
- Class II: Risk 08/21/2025
- Class II: Risk 08/21/2025
- Class II: Risk 08/21/2025
- Class II: Risk 08/21/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.