TriMed — Class II medical device recall Z-1792-2024
Ongoing recall by TriMed Inc., reported 2024-05-22, distributed nationwide. Nail system contains an out of specification driver-socket which could result in inability to pick up nails or
| Recall number | Z-1792-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | TriMed Inc., Santa Clarita, CA, United States |
| Recall initiated | 2024-03-19 |
| Classified | 2024-05-10 |
| Reported by FDA | 2024-05-22 |
| Distributed | Nationwide (US) |
| Quantity | 120 units |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 00842188127885 |
| Lot numbers | QM23087 |
| Model numbers | IMN3.6-60T, IMN3.6-65T |
Product
TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx Only
Reason for recall
Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1792-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.