Ultima Activator II Reusable Drive Mechanism — Class II medical device recall Z-0887-2022
Ongoing recall by Maquet Cardiovascular, LLC, reported 2022-04-13, distributed in AL, AZ, CA, FL, IL, KY, LA, MO…. Potential for corrosion on the pins of the Ultima Activator II Reusable Drive Mechanism. Harms may include all
| Recall number | Z-0887-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Cardiovascular, LLC, Wayne, NJ, United States |
| Recall initiated | 2022-02-09 |
| Classified | 2022-04-06 |
| Reported by FDA | 2022-04-13 |
| Distributed | AL, AZ, CA, FL, IL, KY, LA, MO, MT, NM, OH, PA, TX, WI |
| Countries outside the US | AE, DE, KR, RU, TH |
| Quantity | 60 |
| UPC / GTIN / UDI-DI | 00607567700901 |
| Lot numbers | 25153700, 25157489, 25158616 |
| Model numbers | C-UA-5001, UA-5001 |
Product
Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0887-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.