CLAW II STRAIGHT PLATE ORTHOLOC 3DSi — Class II medical device recall Z-2605-2014
Terminated recall by Wright Medical Technology, Inc., reported 2014-09-17, distributed nationwide. Plates manufactured from an incorrect raw material.
| Recall number | Z-2605-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology, Inc., Memphis, TN, United States |
| Recall initiated | 2014-07-30 |
| Classified | 2014-09-08 |
| Reported by FDA | 2014-09-17 |
| Terminated | 2018-06-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, DE, ES, FR, GB, NL |
| Quantity | 66 units |
| Lot numbers | 1512153, 1518480, 1532497, 1538075, 1538076, 1538332 |
| Model numbers | 40242020 |
Product
CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 20mm x 20mm, REF 40242020, 1 EACH, Rx ONLY, NON STERILE Orthopedic
Reason for recall
Plates manufactured from an incorrect raw material.
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-2605-2014. 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.