Drug recall
Volar Bearing Plate. REF: VBEAL-3-7N, VBEAL-5-7N, VBEAL-3-7S, VBEAL-5-7S, VBEAL-7-7S, VBEAL-3-7W, VBEAL-5-7W…
FDA recall event 93748 · Class II · TriMed Inc.
Key facts
| Event ID | 93748 |
|---|---|
| Recall numbers | Z-0932-2024 |
| Recalling firm | TriMed Inc. |
| Product type | Devices |
| Products | Volar Bearing Plate. REF: VBEAL-3-7N, VBEAL-5-7N, VBEAL-3-7S, VBEAL-5-7S, VBEAL-7-7S, VBEAL-3-7W, VBEAL-5-7W, VBEAR-3-7N, VBEAR-5-7-N, VBEAR-3-7S, VBEAR-5-7S, VBEAR-7-7S, VBEAR-3-7W, VBEAR-5-7W… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Plates, part of a wrist fixation system, are affixed during surgery with bearings that may pop out from distal peg holes. |
| Initiation date | Nov 28, 2023 |
| Report date | Feb 7, 2024 |
| City | Santa Clarita |
| State | CA |
| Country | United States |
| FEI number | 3001236812 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: