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Henry Schein
HENRY SCHEIN, INC. · Model 1045539 · UDI-DI 00304040023358
KAE
Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
225
Facilities
Description
Forceps Ear Dressing Wilde
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
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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.