Maquet Getinge Group Pediatric Arterial Cannula Maquet… — Class II medical device recall Z-2210-2012
Terminated recall by Maquet Inc., reported 2012-08-22, distributed in MI, MN. Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened"
| Recall number | Z-2210-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Inc., Wayne, NJ, United States |
| Recall initiated | 2012-05-29 |
| Classified | 2012-08-15 |
| Reported by FDA | 2012-08-22 |
| Terminated | 2014-04-03 |
| Distributed | MI, MN |
| Lot numbers | 92048923, 92051578 |
| Model numbers | 161412 |
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 info.cp@maquet.com www.maquet.com Used to introduce blood and sterile solution to the circulation system during extracorporeal circulation procedures
Reason for recall
Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip.
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-2210-2012. 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.