FDA Device Intelligence
HomeDevice types › NZJ

Respirator, N95, For Use By The General Public In Public Health Medical Emergencies

FDA product code NZJ · Class 2 · General Hospital

9
Registered devices
4
Adverse events
2
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2020-07-27Office Depot IncTest results revealed that the KN95 masks failed to filter greater than 95% of particulates.
2020-07-02Whirlpool CorporationThe rivets that secure the elastic headband to the face shield have the potential to be mis-assembled. When this condition occurs, it can result in a headband t

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.