Recall: Cardinal Health Infant/Child Reduced Energy Defibrillation Electrodes
On 2017-11-02, the FDA announced that Physio-Control is conducting a recall on Infant/Child Reduced Energy Defibrillation Electrodes due to a possible defect. The recalled products were sold under the brand name(s) Cardinal Health during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 3 medical devices recalls due to potential defect, including catheters, infusion sets and more. Additionally, there have been 1 drug and medical device recalls due to other health hazards as well as 109 food recalls.
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Detailed Recall Information
Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.
Product Description: Infant/Child Reduced Energy Defibrillation Electrodes
Brand Name(s): Cardinal Health
Reason for Recall: Incorrect artwork on the defibrillation electrodes within the packaging
Official Recall Date: 2017-10-27
Note: Although this recall announcement is dated 10/27/2017, it was not published by the FDA until 11/02/2017.
Additional information provided by the FDA.gov:
Physio-Control announced today that the company is launching a voluntary field action for specific production lots of Infant/Child Reduced Energy Defibrillation Electrodes (defibrillation electrodes) produced by Cardinal Health. 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.