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ELMED
ELMED INCORPORATED · Model 55-919 · UDI-DI 00842180176294
FNY
Prescription
9
510(k) clearances
12
Adverse events
1
Recalls
224
Facilities
Description
EMESIS BASIN 8-1/2 X 3-5/8 X 1-5/8"
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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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.