Recall: ThermaCare Back Pain Therapy HeatWraps
On 2019-04-26, the FDA announced that Pfizer is conducting a recall on Back Pain Therapy HeatWraps due to a possible . The recalled products were sold under the brand name(s) ThermaCare during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 1 medical devices recalls due to potential undetermined hazard, including temporary bipolar pacing lead, model tb, maquet/getinge cardiosave intra-aortic balloon pumps (iabp) and more. Additionally, there have been 1 drug and medical device recalls due to other health hazards as well as 80 food recalls.
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Detailed Recall Information
Regions Where Sold: Nationwide
Product Description: Back Pain Therapy HeatWraps
Brand Name(s): ThermaCare
Reason for Recall: Undetermined Hazard
Official Recall Date: 2019-04-26
Additional information provided by the FDA.gov:
Pfizer Consumer Healthcare, a division of Pfizer Inc., is voluntarily recalling one lot of ThermaCare Back Pain Therapy HeatWraps, up to 16HR pain relief, to the consumer level. Pfizer Consumer Healthcare initiated this recall due to the potential that a HeatWrap could include cells that have a higher cell temperature than specified. Read More.
More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.