CONAIR
Received May 30, 2025 · Event occurred Dec 23, 2024
Report 1222304-2025-00002 · MDR key 22113076
Device
Product problems
- Insufficient Device Problem Information
- Insufficient Device Problem Information
Patient
NA · Unknown
- Insufficient Information
- Insufficient Information
Narrative
Additional Manufacturer Narrative
1/23/2025 - WE HAVE REQUESTED THE DEVICE BE RETURNED FROM THE CONSUMER. TO DATE, WE HAVE NOT RECEIVED THE DEVICE. 3/6/2025 - IT WAS DISCOVERED AN ERROR IN THE FDA MANUFACTURER NUMBER WAS INCORRECT. RESUBMITTING AN SUPPLEMENTAL EMDR WITH THE CORRRECT FDA MANUFACTURER NUMBER. THE ORIGINAL MANUFACTURER REPORT NUMBER WAS 1222301-2020-00002. THE CORRECT MANUFACTURER NUMBER SHOULD BE 1222304-2025-00002. THE INITIAL MDR WAS SUBMITTED VIA THE OLDER ESG SYSTEM AND WILL BE RESUBMITTING VIA THE NEW ESG SYSTEM AS AN INITIAL REPORT.
Description of Event or Problem
1/23/2025 - THE CONSUMER CLAIMS THE PRODUCT HAD A BURNT SMELL.