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Henry Schein
HENRY SCHEIN, INC. · Model 1045767 · UDI-DI 00304040016220
KAI
Prescription
9
510(k) clearances
4
Adverse events
1
Recalls
109
Facilities
Description
Mirror Laryngeal w/o Handle
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
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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.