PATH — Class II medical device recall Z-1712-2014
Terminated recall by Microport Orthopedics INC., reported 2014-06-11, distributed nationwide. Difficulty removing the cup adaptor from the impaction handle during surgery
| Recall number | Z-1712-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microport Orthopedics INC., Arlington, TN, United States |
| Recall initiated | 2014-04-30 |
| Classified | 2014-06-04 |
| Reported by FDA | 2014-06-11 |
| Terminated | 2014-12-01 |
| Distributed | Nationwide (US) |
| Quantity | 140 units |
| Lot numbers | 1153896, 1279714, 1288604, 1314793 |
| Model numbers | 2007-0013 |
Product
PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument.
Reason for recall
Difficulty removing the cup adaptor from the impaction handle during surgery
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-1712-2014. 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.