FDA Adverse Event Other Summary report: N

ICY HOT HEAT THERAPY PATCH

MDR report key: 1014202 · Received March 13, 2008

Report

Report Number
1022556-2008-00229
Event Type
Other
Date Received
March 13, 2008
Report Date
February 13, 2008
Manufacturer
CHATTEM, INC.
Product Code
IMD
Removal / Correction Number
Z-1196-2008
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

PACKAGE LABELING INDICATES THAT CONSUMERS SHOULD CONSULT WITH THEIR DOCTOR BEFORE USE IF THEY HAVE DIABETES. SINCE THIS IS A DISPOSABLE SINGLE-USE DEVICE, THE PATCH IS UNAVAILABLE FOR EVALUATION AND ANALYSIS. THE LOT NUMBER WAS NOT PROVIDED FROM THE REPORTER TO CONDUCT TREND ANALYSIS. THIS REPORT IS BELOW THE THRESHOLD OF THE FDA'S REQUIREMENTS FOR MANDATORY REPORTING OF ADVERSE EVENTS INVOLVING MEDICAL DEVICES, AS THERE IS NO EVIDENCE THAT USE OF THE PRODUCT RESULTED IN SERIOUS ADVERSE HEALTH CONSEQUENCES. INSTEAD, OUR INVESTIGATION HAS DETERMINED THAT THE PATIENT EXPERIENCED TEMPORARY OR MEDICALLY REVERSIBLE ADVERSE HEALTH CONSEQUENCES. ACCORDINGLY, THIS MDR IS BEING SUBMITTED AS A VOLUNTARY AND PROACTIVE MEASURE BY THE MFR TO ENHANCE PRODUCT SAFETY AND PHARMACOVIGILANCE.

Description of Event or Problem · 1

THE CONSUMER REPORTED, USING THE PRODUCT FOR FIVE HRS ON HER SHOULDER. WHEN THE PATCH WAS REMOVED, THE CONSUMER DESCRIBED REDNESS, AND A BURN IN THE AREA WORN WHICH HAS SCABBED OVER AND IS HEALING. THE CONSUMER DID NOT SEEK MEDICAL ATTENTION AT THE TIME OF THE INCIDENT AND TREATED THE AREA BY SOAKING IN A BATH AND KEEPING CLEAN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ICY HOT HEAT THERAPY PATCH IMD CHATTEM, INC. 083

Patients

Seq Age Sex Outcome Treatment
1 73 YR THE CONSUMER REPORTED TAKING UNSPECIFIED HEART| AND DIABETIC MEDICATIONS AT THE TIME OF THE| INCIDENT.