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SR PIP
Stryker GmbH · Model 17-1364 · UDI-DI 00886385020105
MPK
Prescription
0
510(k) clearances
120
Adverse events (1 deaths)
1
Recalls
5
Facilities
Description
Trial Extractor, SR PIP
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-07-27 | Wright Medical Technology, Inc. | An incorrect sizing label was applied to the carton packaging. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.