Recall: ATAR Extension Cable
On 2017-07-06, the FDA announced that Oscor is conducting a recall on Extension Cable due to a possible defect. The recalled products were sold under the brand name(s) ATAR during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 5 medical devices recalls due to potential defect, including catheters, intra-aortic balloon pumps and more. Additionally, there have been 3 drug and medical device recalls due to other health hazards as well as 141 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: Extension cable
Brand Name(s): ATAR
Reason for Recall: Cable may separate from the connector at the proximal end
Official Recall Date: 2017-07-06
Additional information provided by the FDA.gov:
The extension cable is intended to connect an electrode/lead from a patient or another cable to a diagnostic machine or an external pacemaker. Read More.
More information may be available at FDA.gov
Latest Safety Recalls
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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.