Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Thoratec CentriMag Motor Recalled by Thoratec Switzerland GMBH Due to Reports of circulatory support system motor stopping. Motor...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Thoratec Switzerland GMBH directly.
Affected Products
Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood Pumping System.
Quantity: 1569
Why Was This Recalled?
Reports of circulatory support system motor stopping. Motor stop can be attributed to a break of a wire or short circuit between wires within the electrical cable where the cable exits the motor cable bend protection.
Where Was This Sold?
This product was distributed to 43 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WV, WI, DC
About Thoratec Switzerland GMBH
Thoratec Switzerland GMBH has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report