InjuryMSH
HALYARD N95 MASK
Received Sep 28, 2020 · Event occurred Sep 25, 2020
Report MW5096923 · MDR key 10600258
Device
Generic name
Respirator, Surgical
Manufacturer
BattelleProduct problems
- Adverse Event Without Identified Device or Use Problem
Patient
Not reported
- Dyspnea
- Irritation
- Cough
- Dyspnea
- Irritation
- Cough
Narrative
Description of Event or Problem
IRRITATED THROAT, SHORTNESS OF BREATH, COUGHING, CHOKING FEELING NOTED 1HR AFTER DONNING BATTELLE REPROCESSED N95 (PRESTIGE AMERICA). FDA SAFETY REPORT ID# (B)(4).