Class II — Folsom Metal Products, Inc.
| Recalling firm | Folsom Metal Products |
|---|---|
| Registered facility | FOLSOM METAL PRODUCTS, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Labeling includes shelf life that has not been validated. |
| Product | Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 10 single packs , Rx Only, Sterile |
| Quantity | 10,960 units |
| Distribution | US Nationwide distribution in the states of AL, CA, FL, GA, IL, MD, MI, PA, TX. |
| Initiated | 2025-08-21 |
| Classified | 2025-09-17 |
| Recall number | Z-2579-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Folsom Metal Products, Inc. (Z-2579-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97480/
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