Class II — Maquet Inc.
| Recalling firm | MAQUET (Suzhou) Co., Ltd |
|---|---|
| Registered facility | MAQUET (SUZHOU) CO., LTD (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip. |
| Product | Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone +49 7222 932-0 Fax: +49 7222 932-1888 [email protected] www.maquet.com Used to introduce blood and sterile solution to the circulation system during extracorporeal circulation procedures |
| Quantity | 20 devices US; 122 devices foreign |
| Distribution | Worldwide Distribution - USA including MI, MN and Internationally |
| Initiated | 2012-05-29 |
| Classified | 2012-08-15 |
| Terminated | 2014-04-03 |
| Recall number | Z-2210-2012 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Maquet Inc. (Z-2210-2012).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/62471/
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