PROFEMUR PLUS CoCr MODULAR NECK — Class I medical device recall Z-2743-2015
Terminated recall by MicroPort Orthopedics, Inc., reported 2015-10-07, distributed nationwide. Unexpected rate of postoperative fractures resulting in the need for revision surgery.
| Recall number | Z-2743-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MicroPort Orthopedics, Inc., Arlington, TN, United States |
| Recall initiated | 2015-08-04 |
| Classified | 2015-09-28 |
| Reported by FDA | 2015-10-07 |
| Terminated | 2018-08-17 |
| Distributed | Nationwide (US) |
| Quantity | 10,489 units |
| Reason classes | device malfunction |
| Model numbers | PHAC1254 |
Product
PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree VAR/VAL. 12/14 SLT Taper. Orthopedic hip prosthesis component.
Reason for recall
Unexpected rate of postoperative fractures resulting in the need for revision 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-2743-2015. 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.