Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW — Class II medical device recall Z-2032-2014
Terminated recall by Zimmer Manufacturing B.V., reported 2014-07-16, distributed nationwide. Two lots of screws were commingled. Screws with etching and machining for lot number 62629432 were packaged in
| Recall number | Z-2032-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Manufacturing B.V., Mercedita, PR, United States |
| Recall initiated | 2014-06-12 |
| Classified | 2014-07-10 |
| Reported by FDA | 2014-07-16 |
| Terminated | 2015-06-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CN, IN, JP |
| Quantity | 496 |
| Reason classes | labeling |
| Lot numbers | 62628759, 62629432 |
Product
Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW, FULLY THREADED, HEX HEAD 4MM DIAMETER, 14 MM LENGTH, and EDI 4.0 MM CANCELLOUS SCREW, FULLY THREADED, 20 MM LENGTH. Temporary internal fixation devices, designed to stabilize fractures during the normal healing process.
Reason for recall
Two lots of screws were commingled. Screws with etching and machining for lot number 62629432 were packaged in bags labeled for lot number 62628759; and screws with etching and machining for lot number 62628759 were packaged in bags labeled for lot number 62629432. The affected product was distributed between 3/6/14 and 4/21/14.
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-2032-2014. 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.