FDA Adverse Event Injury Summary report: N

INSTANT HOT PACK

MDR report key: 17184627 · Received June 21, 2023

Report

Report Number
MW5118684
Event Type
Injury
Date Received
June 21, 2023
Date of Event
June 14, 2023
Report Date
June 16, 2023
Manufacturer
DYNAREX CORPORATION
Product Code
IMD
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
NY, US
Reporter Occupation
117
Health Professional
Yes

Narratives

Description of Event or Problem · 0

PATIENT BURNED FROM HOT PACK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1758572 INSTANT HOT PACK PACK, HOT OR COLD, DISPOSABLE IMD DYNAREX CORPORATION 53654

Patients

Seq Age Sex Outcome Treatment
1 Unknown Other