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Home > Recalled Products > Medical Devices > Defect > Lifepak 15 Monitor/Defibrillator

Recall: Lifepak 15 Monitor/Defibrillator

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On 2019-02-01, the FDA announced that Stryker is conducting a recall on 15 Monitor/Defibrillator due to a possible defect. The recalled products were sold under the brand name(s) Lifepak during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 2 medical devices recalls due to potential defect, including roche coaguchek test strips, temporary bipolar pacing leads and more. Additionally, there have been 2 drug and medical device recalls due to other health hazards as well as 74 food recalls.

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Stryker, Logo
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Company Contact Information:

Name: Stryker
Website: www.stryker.com
Phone: 1-800-442-1142

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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: 15 Monitor/Defibrillator

Brand Name(s): Lifepak

Reason for Recall: Defect

Official Recall Date: 2019-02-01


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Additional information provided by the FDA.gov:

Stryker announced today that the company is launching a voluntary field action on specific units of the LIFEPAK 15 Monitor/Defibrillators. 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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