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Smith & Nephew, Inc. · Model 72200315S · UDI-DI 03596010606709
FEI
Prescription
2
510(k) clearances
19
Adverse events
2
Recalls
35
Facilities
Description
19.5 MM HIGH DEFINITION ENDOCOUPLER, C-MOUNT, BLACK RING - 560H HEAD ONLY, SERVICE REPLACEMENT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-10-04 | Medtronic | Product sterility is compromised due to breach of the sterile barrier |
| 2016-10-04 | Medtronic | Product sterility is compromised due to breach of the sterile barrier |
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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.