Lower riskMedical device recall · FDA · Published February 9, 2022
Maquet Ultima Activator II Drive Mechanism Recall: Corrosion Risk
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 Ultima Activator II Drive Mechanism Recall: Corrosion Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61164-maquet-ultima-activator-ii-drive-mechanism-recall-corrosion-risk. Based on FDA recall #Z-0887-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0887-2022%22&limit=1).
The FDA announced on Feb. 9, 2022, that Maquet Cardiovascular, LLC is recalling the Ultima Activator II Reusable Drive Mechanism due to potential corrosion on its pins. Owners should contact the company for a replacement or repair.
How to tell if you have it
Brand: Maquet
Product: Ultima Activator II Reusable Drive Mechanism
Part #: C-UA-5001
Labeled REF: UA-5001
UDI#: 00607567700901
Lot codes: 25153700, 25157489, 25158616
The hazard
The recall cites potential corrosion on the pins of the Ultima Activator II Reusable Drive Mechanism. Harms may include allergic reaction, metal toxicity, and other delayed responses.
Context
GovInfoNow's records show Maquet Cardiovascular, LLC has 25 other recalls on record since Jan. 24, 2019. Other recent recalls of similar products include Oculus PhaseOne Antimicrobial Solution Recall (April 27, 2026), Kico Arvis Hip & Knee 3.0 Instrument Set Recall (April 23, 2026), and Codman Microsensor Basic Kit Recall (Dec. 12, 2025).
How to tell if you have this one
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.
Brand
Maquet
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Package
Look for lot numbers 25153700, 25157489, or 25158616 on the device package.
Inspect Handle for Lot Number
If packaging is discarded, check for Device Component Lot number (200501) etched on the handle and pin areas.
Where it went and when
Where it was distributed
Distributed in 14 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “Worldwide - United States (AL, AZ, CA, FL, IL, KY, LA, MO, MT, NM, OH, PA, TX, WI), Germany, Republic of Korea (South Korea), Russia, Thailand, United Arab Emirates.” States read from FDA’s own wording; “not listed” means the notice does not name it.
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.
Official source: FDA Recall #Z-0887-2022 (February 9, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0887-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.