Recall: Lifepak 15 Monitor/Defibrillator
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.
Company Contact Information:
Do you work for a company involved with this recall? Contact us to learn how you can control data, information and ads shown on this page.
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
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
Latest Safety Recalls
Select image for details, including additional styles.
Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.