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KN95 FACE MASK Adverse Event — Injury (MDR MW5094282)

KN95 FACE MASK Adverse Event — Injury (MDR MW5094282) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: KN95 FACE MASK; Generic name: RESPIRATOR, SURGICAL; Manufacturer: GUANGDONG ZHIZHEN BIOLOGICAL MEDICINE CO., LTD..

DeviceKN95 FACE MASK
Generic nameRESPIRATOR, SURGICAL
ManufacturerGUANGDONG ZHIZHEN BIOLOGICAL MEDICINE CO., LTD.
Report numberMW5094282
Event typeInjury
Product problemY
Date received2020-04-27
NarrativeFRAUDULENT FACE MASK WITH HOLES THROUGH MASK, FDA LOGO AND KN95 STAMP WITH HOLES THROUGH MASK. FDA SAFETY REPORT ID# (B)(4).
SourceopenFDA MAUDE (device adverse events)

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