MAQUET GETINGE GROUP Arterial Cannula OD Used to introduce blood and… — Class II medical device recall Z-1572-2013
Terminated recall by Maquet Cardiovascular Us Sales, Llc, reported 2013-07-03, distributed in DE, IL, MN, NY, OH, PA. The specified part numbers and lot numbers of Maquet Pediatric Arterial Cannula Packs may contain an incorrect
| Recall number | Z-1572-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Cardiovascular Us Sales, Llc, Wayne, NJ, United States |
| Recall initiated | 2013-05-14 |
| Classified | 2013-06-21 |
| Reported by FDA | 2013-07-03 |
| Terminated | 2014-09-18 |
| Distributed | DE, IL, MN, NY, OH, PA |
| Countries outside the US | DE, FR, TR |
Product
MAQUET GETINGE GROUP Arterial Cannula OD Used to introduce blood and sterile solutions into the systemic circulation during pediatric extracorporeal circulation procedures.
Reason for recall
The specified part numbers and lot numbers of Maquet Pediatric Arterial Cannula Packs may contain an incorrectly sized connector.
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-1572-2013. 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.