FDA Device recall Z-2743-2015
PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree VAR/VAL. 12/14 SLT Taper
- FDA Device
- Class I
- terminated
- Published 2015-10-07
On 2015-10-07 the FDA classified a Class I recall of PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree VAR/VAL. 12/14 SLT Taper by Microport Orthopedics, citing unexpected rate of postoperative fractures resulting in the need for revision surgery.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2743-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-08-04 |
| Published | 2015-10-07 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Microport Orthopedics |
| Distribution | US |
Product
PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree VAR/VAL. 12/14 SLT Taper. Orthopedic hip prosthesis component.
Reason
Unexpected rate of postoperative fractures resulting in the need for revision surgery.
Identifiers
| code_info | All lot codes |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2743-2015%22
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