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Maquet Inc. recalls Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phon
Recalled August 22, 2012 · FDA recall Z-2210-2012 · Maquet
Hazard
Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip. · FDA Class II
Units
20 devices US; 122 devices foreign
Sold at
Worldwide Distribution - USA including MI, MN and Internationally
Description
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
Manufacturer(s)
Maquet Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →