FDA Recall Open, Classified

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

Recall: Z-2577-2025 · Initiated August 21, 2025

Recall

Recall Number
Z-2577-2025
Event Number
97480
Firm
Folsom Metal Products, Inc.
FEI Number
3006803588
Product Code
GCZ
Status
Open, Classified
Root Cause
Incorrect or no expiration date
Initiated
August 21, 2025
Posted
September 17, 2025
Address
1449 Court Pl, Pelham, AL, 35124-1858

Description

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.

Action

On August 21, 2025, Frortier Devices issued a "Urgent: Medical Device Recall" Notification to affected consignees via FedEx. On August 22, 2025, Frontier reissued the notification to correct an incorrect product number. Frontier asked consignees to take the following actions: 1. Immediately examine your inventory and quarantine any affected units. 2.If you have affected units: Return product to Frontier Devices at the address listed, OR Destroy product on-site and complete the enclosed Certificate of Destruction Form. 3. If you may have further distributed this product, please identify your customers and notify them at once of this product recall. Your notification to your customers may be enhanced by including a copy of this recall notification letter. Please share this notice with all users within your organization. If the product has been transferred to a different facility, please make them aware of the notice. 4. Complete and return the enclosed Medical Device Recall Response Acknowledgment Form as soon as possible, even if no affected product remains in your possession. Please have them complete the acknowledgement response form and return it to you.

Distribution

US Nationwide distribution in the states of AL, CA, FL, GA, IL, MD, MI, PA, TX.

Quantity

160 units