Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ultima Activator II Reusable Drive Mechanism Recalled by Maquet Cardiovascular, LLC Due to Potential for corrosion on the pins of the...
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 Maquet Cardiovascular, LLC directly.
Affected Products
Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.
Quantity: 60
Why Was This Recalled?
Potential for corrosion on the pins of the Ultima Activator II Reusable Drive Mechanism. Harms may include allergic reaction, metal toxicity, and other delayed responses.
Where Was This Sold?
This product was distributed to 14 states: AL, AZ, CA, FL, IL, KY, LA, MO, MT, NM, OH, PA, TX, WI
About Maquet Cardiovascular, LLC
Maquet Cardiovascular, LLC has 251 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report