ICY HOT HEAT THERAPY PATCH
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
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.
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. |