Recall Z-2577-2025— Folsom Metal Products, Inc.

Class II · Ongoing

Class II FDA medical device recall by Folsom Metal Products, Inc., initiated 2025-08-21. FDA's recall record names no specific 510(k) clearance for this event. Product: Frontier Devices, REF: 301.912S2, 12 mm Distraction Pin, 10 double packs , Rx Only, Sterile. Reason: Labeling includes shelf life that has not been validated..

Recalling firm
Folsom Metal Products, Inc.
Classification
Class II
Status
Ongoing
Initiated
2025-08-21
Firm location
Pelham, AL, United States

Product description

Frontier Devices, REF: 301.912S2, 12 mm Distraction Pin, 10 double packs , Rx Only, Sterile

Reason for recall

Labeling includes shelf life that has not been validated.

Data sourced from openFDA. This site is unofficial and independent of the FDA.