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Henry Schein
HENRY SCHEIN, INC. · Model 5701883 · UDI-DI 20304040127869
9
510(k) clearances
12
Adverse events
1
Recalls
224
Facilities
Description
Ear Wash Tips, 20 Tips
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-05-30 | DeRoyal Industries Inc | The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside. |
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
