Maquet recalls Ultima Activator II Reusable Drive Mechanism part # C-UA-5001 due to potential corrosion causing allergic reactions and metal toxicity. Affected lots: 25153700, 25157489, 25158616.
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.
Maquet is recalling the Ultima Activator II Reusable Drive Mechanism part # C-UA-5001 because corrosion on its pins could cause allergic reactions or metal toxicity. This affects specific lots of the device used in medical procedures.
Corrosion on the pins can lead to allergic reactions or metal toxicity over time. This happens because the metal components may react with bodily fluids or tissues during medical procedures.
Medical professionals using the Ultima Activator II device in procedures are most at risk. Patients receiving treatments with this device may also be affected if the corrosion causes reactions.
Check the device package for lot numbers 25153700, 25157489, or 25158616. If packaging is discarded, look for the Device Component Lot number (200501) etched on the handle and pin areas.
Look for lot numbers 25153700, 25157489, or 25158616 on the device package.
If packaging is discarded, check for Device Component Lot number (200501) etched on the handle and pin areas.
The Ultima Activator II Reusable Drive Mechanism part # C-UA-5001 (labeled REF UA-5001).
Check the device package for lot numbers 25153700, 25157489, or 25158616. If packaging is discarded, look for Device Component Lot number (200501) on the handle and pin areas.
The recall record does not specify a remedy.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-0887-2022 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-0887-2022 from Maquet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
