FDA Device recall Z-1712-2014
PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc
- FDA Device
- Class II
- terminated
- Published 2014-06-11
On 2014-06-11 the FDA classified a Class II recall of PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc by Microport Orthopedics, citing difficulty removing the cup adaptor from the impaction handle during surgery.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1712-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-30 |
| Published | 2014-06-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Microport Orthopedics |
| Distribution | US |
Product
PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument.
Reason
Difficulty removing the cup adaptor from the impaction handle during surgery
Identifiers
| code_info | Lot Number(s): 1153896, 1279714, 1288604, and 1314793 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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All Microport Orthopedics recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1712-2014%22
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