Zimmer Periarticular Locking Plate System Distal Radial Volar Plate… — Class II medical device recall Z-2131-2014
Terminated recall by Zimmer, Inc., reported 2014-08-06, distributed in CA, OH. A complaint was received in which it was reported that an 8-hole plate from lot 62276042 had an enlarged hole
| Recall number | Z-2131-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-06-10 |
| Classified | 2014-07-30 |
| Reported by FDA | 2014-08-06 |
| Terminated | 2015-01-09 |
| Distributed | CA, OH |
| Countries outside the US | BR, CN, KR, TW |
| Quantity | 28 units |
| Lot numbers | 62276042 |
| Model numbers | 00-2358-014-04 |
Product
Zimmer Periarticular Locking Plate System Distal Radial Volar Plate Lateral Column (1st generation stainless steel only). Orthopedic fixation plate. For temporary internal fixation and stabilization of osteotomies and fractures.
Reason for recall
A complaint was received in which it was reported that an 8-hole plate from lot 62276042 had an enlarged hole that is unable to lock the screw, which resulted in the screw head pulling through plate hole.
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-2131-2014. 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.