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Home > Recalled Products > Medical Devices > Undetermined Hazard > SAM Extremity Tourniquets

Recall: SAM Extremity Tourniquets

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On 2018-05-01, the FDA announced that SAM Medical is conducting a recall on Extremity Tourniquets due to a possible undetermined hazard. The recalled products were sold under the brand name(s) SAM 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 zenith alpha thoracic endovascular graft ‎products, nc trek rx coronary dilatation catheter, nc traveler coronary dilatation catheter, and nc tenku rx ptca balloon catheter and more. Additionally, there have been 1 drug and medical device recalls due to other health hazards as well as 93 food recalls.

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Product image of Affected tourniquet with no box stitch
Note: Images may not be available for every version. Please review the detailed description below.

Company Contact Information:

Name: SAM Medical
Website: www.sammedical.com
Phone: 1 800- 580-3519

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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: Extremity Tourniquets

Brand Name(s): SAM

Reason for Recall: Undetermined Hazard

Official Recall Date: 2018-05-01


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Additional information provided by the FDA.gov:

SAM Medical today announced it is conducting a voluntary international recall of all unused SAM XT Extremity Tourniquets (SAM XT). The company initiated the recall after internal testing indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. To date, there have been no reports of adverse health consequences received. This recall is being made with the knowledge of the Food and Drug Administration and other relevant Competent Authorities. 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.

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