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HALYARD
GRI Medical & Electronic Technology Co., Ltd. · Model 68483-80 · UDI-DI 16931918178516
9
510(k) clearances
12
Adverse events
1
Recalls
224
Facilities
Description
Drawcord Bag_Clear_54inx42in_1.8mil_N/S_50ea/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.