FDAFebruary 9, 2022device
Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Ongoing
Brands named
maquet cardiovascularmaquet
UPCs
00607567700901
Recall history
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