FDA Adverse Event Malfunction Summary report: N

NA

MDR report key: 10777575 · Received November 3, 2020

Report

Report Number
1523658-2020-00036
Event Type
Malfunction
Date Received
November 3, 2020
Date of Event
April 26, 2020
Report Date
November 2, 2020
Manufacturer
BATTELLE MEMORIAL INSTITUTE
Product Code
QLA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE NOT RETURNED. CCDS AND HOSPITAL STAFF HAVE DISCUSSED THE ISSUES REGARDING THE RETURNED MASKS. INFORMATION REQUIRING THE EVALUATION FOR MASK SOILING AND STRAP INTEGRITY WHEN LOADING AND UNLOADING INTO CHAMBERS HAS BEEN DISPERSED TO SITES.

Description of Event or Problem · 1

USER REPORTED STRAP ON MASK BROKE. THE MASKS ASSOCIATED WITH THIS EVENT WERE DECONTAMINATED WITH THE BATTELLE CCDS "CLOSED SYSTEM" PROCESS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1246828 NA RESPIRATOR, DECONTAMINATED QLA BATTELLE MEMORIAL INSTITUTE

Patients

Seq Age Sex Outcome Treatment
1