FDA Adverse Event Other Summary report: N

THERABATH

MDR report key: 497999 · Received July 18, 2003

Report

Report Number
2118418-2003-00001
Event Type
Other
Date Received
July 18, 2003
Date of Event
February 16, 2001
Report Date
July 18, 2003
Manufacturer
WR MEDICAL ELECTRONICS CO.
Product Code
IMC
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PT MAY HAVE DAMAGE TO SMALL CUTANEOUS FIBERS IN THEIR FEET BROUGHT ON BY PARAFFIN TREATMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 THERABATH PARAFFIN HEAT THERAPY BATH IMC WR MEDICAL ELECTRONICS CO. TB II NA

Patients

Seq Age Sex Outcome Treatment
1 44 YR Other