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Alleset
GRI Medical & Electronic Technology Co., Ltd. · Model Model 19-1070B-RD · UDI-DI 16931918157979
9
510(k) clearances
11
Adverse events
1
Recalls
224
Facilities
Description
Waste Containment Bowl_Red_Bulk_non-sterile_200ea/cs
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.