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..
| Device | KN95 FACE MASK |
|---|---|
| Generic name | RESPIRATOR, SURGICAL |
| Manufacturer | GUANGDONG ZHIZHEN BIOLOGICAL MEDICINE CO., LTD. |
| Report number | MW5094282 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | FRAUDULENT FACE MASK WITH HOLES THROUGH MASK, FDA LOGO AND KN95 STAMP WITH HOLES THROUGH MASK. FDA SAFETY REPORT ID# (B)(4). |
| Source | openFDA MAUDE (device adverse events) |
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