CROSSCHECK — Class II medical device recall Z-1485-2015
Terminated recall by Wright Medical Technology, Inc., reported 2015-04-29, distributed nationwide. The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which
| Recall number | Z-1485-2015 |
|---|---|
| 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 | 2015-03-06 |
| Classified | 2015-04-22 |
| Reported by FDA | 2015-04-29 |
| Terminated | 2018-08-05 |
| Distributed | Nationwide (US) |
| Quantity | 102 units |
| Reason classes | specification failure, device malfunction |
| Lot numbers | 35049-31A-1, 35049-3A, 35049-3A-1-1, 36281-2-1, 362812 |
| Model numbers | CCP-LPX0R |
Product
CROSSCHECK(R) Plating system, LAPIDUS CX Plate, NEUTRAL, Right, REF CCP-LPX0R. Orthopedic use.
Reason for recall
The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction
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-1485-2015. 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.