Class II — Microport Orthopedics INC.
| Recalling firm | MicroPort Orthopedics Inc. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Difficulty removing the cup adaptor from the impaction handle during surgery |
| Product | PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument. |
| Quantity | 140 units |
| Distribution | Nationwide Distribution. |
| Initiated | 2014-04-30 |
| Classified | 2014-06-04 |
| Terminated | 2014-12-01 |
| Recall number | Z-1712-2014 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Microport Orthopedics INC. (Z-1712-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68326/
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