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Maquet Cardiovascular Us Sales, Llc recalls MAQUET GETINGE GROUP Arterial Cannula OD Used to introduce blood and sterile solutions into the systemic circulation

Recalled July 3, 2013 · FDA recall Z-1572-2013 · Maquet Cardiovascular Us Sales

Hazard
The specified part numbers and lot numbers of Maquet Pediatric Arterial Cannula Packs may contain an incorrectly sized connector. · FDA Class II
Units
100 units (60 Domestic; 40 International)
Sold at
Worldwide Distribution - US Distribution including the states of Delaware, Illinois, Minnesota , New York., Ohio and Pennsylvania and the countries of Germany, Turkey and France.

Description

The specified part numbers and lot numbers of Maquet Pediatric Arterial Cannula Packs may contain an incorrectly sized connector.

Product
MAQUET GETINGE GROUP Arterial Cannula OD Used to introduce blood and sterile solutions into the systemic circulation during pediatric extracorporeal circulation procedures.
Manufacturer(s)
Maquet Cardiovascular Us Sales, Llc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Maquet Cardiovascular Us Sales, Llc recalls MAQUET GETINGE GROUP Arterial Cannula OD Used to introduce blood and sterile solutions into the systemic circulation | RecallWatchUSA