FDA Adverse Event Injury Summary report: N

MASK

MDR report key: 11854696 · Received May 19, 2021

Report

Report Number
MW5101430
Event Type
Injury
Date Received
May 19, 2021
Date of Event
May 17, 2021
Report Date
May 17, 2021
Manufacturer
UNK
Product Code
QKR
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I AM REQUIRED TO WEAR I MASK AT WORK. I CONTINUALLY SUFFER FROM HEADACHES, MIGRAINES, SHORTNESS OF BREATH, FATIGUE AND OVERHEATING. FDA SAFETY REPORT ID # (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
742842 MASK FACE MASK PER ENFORCEMENT POLICY FOR FACE MASKS AND RESPIRATORS DURING THE COVID QKR UNK

Patients

Seq Age Sex Outcome Treatment
1 Disability