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R3
Smith & Nephew, Inc. · Model E0015118-7 · UDI-DI 00885556653418
LPO
Prescription
1
510(k) clearances
508
Adverse events
1
Recalls
3
Facilities
Description
MODIFIED +4MM OFFSET TRIAL HEAD SZ36MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-11-18 | Alcon Laboratories, Inc | The firm initiated the recall on 11/18/2003 via letters to all consignees. The letter advises physicians to stop using any patient bracelets (blue color) that contain the word 'st |
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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.