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Alleset
GRI Medical & Electronic Technology Co., Ltd. · Model DTCL4040 · UDI-DI 16931918185460
9
510(k) clearances
12
Adverse events
1
Recalls
226
Facilities
Description
Draw_Tape_Bag_40in x40in_Clear_bulk_non-sterile_100ea/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.