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HALYARD

GRI Medical & Electronic Technology Co., Ltd. · Model 68494-80 · UDI-DI 16931918157375

FNY
9
510(k) clearances
12
Adverse events
1
Recalls
224
Facilities

Description

Trash Liner_Clear_33inx38in_1mil_N/S_250ea/cs

Recalls

DateFirmReason
2023-05-30DeRoyal Industries IncThe outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.