Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2210-2012 — 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 circula

U.S. FDA — Device Enforcement · United States · 2012-05-29 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2210-2012
Date of alert: 2012-05-29
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Maquet Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 92048923

Reported risk: Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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