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Peri-loc
Smith & Nephew, Inc. · Model E0014841-7 · UDI-DI 00885556616802
HXZ
Prescription
1
510(k) clearances
514
Adverse events
1
Recalls
247
Facilities
Description
K-WIRE WITH LOOP END
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-20 | Zimmer Biomet, Inc. | Device has the potential for fracture during use. |
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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.