FDA Adverse Event
Malfunction
Summary report: N
NA
MDR report key: 10801523
·
Received November 6, 2020
Report
- Report Number
- 1523658-2020-00197
- Event Type
- Malfunction
- Date Received
- November 6, 2020
- Report Date
- November 6, 2020
- Manufacturer
- BATTELLE MEMORIAL INSTITUTE
- Product Code
- QKY
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
DEVICE NOT RETURNED. CCDS STAFF HAS BEEN IN CONTACT WITH HCP, EXPLAINING THE DECONTAMINATION PROCESS, THE CHEMICALS USED (SDSS), AND PROVIDED A LINK TO FAQS FOR HCPS AS WELL AS SUGGESTING AIRING OUT THE MASKS PRIOR TO USE.
Description of Event or Problem · 1
USER REPORTED CHEMICAL ODOR. 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 |
|---|---|---|---|---|---|---|---|
| 1265458 | NA | RESPIRATOR, DECONTAMINATED | QKY | BATTELLE MEMORIAL INSTITUTE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |