The root cause cannot be identified.There is limited device specific information provided, no batch number was available for evaluation.Without a batch reference number, a manufacturing and technical evaluation cannot be completed for the wrap involved in this case.No product quality related trend was identified for the subclass adverse event safety request for investigation.Care should be taken when using the device, following all safety and use information as provided with the wrap to avoid the risk of blisters and other skin irritations.The manufacturing operations employ quality control procedures which include in process testing, thermal testing and visual inspection, to ensure packaged product quality.There are pre-identified risk factors that could cause a burn listed in the hazard analysis (rpt-000097160).In addition to these hazards, there are multiple risks that are outside the control of the site.These include things like age, skin condition, medical conditions, device use error and off-label use.The warning labels on our product are used to address these risks and relay the appropriate instructions for use to our customers to avoid burns, blisters and skin irritations.
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On 17-oct-2023, a spontaneous report from the united states was received via email regarding a female (age not provided) who used a thermacare menstrual 8hr heat wrap.On an unspecified date, the consumer topically applied a thermacare menstrual 8hr heat wrap for an unspecified indication.On an unspecified date after using the product, the consumer experienced a burn.Her skin was fried and painful.No additional information was provided.
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