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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
Recall Date to: 07/28/2014 510(K) Number: K041223
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FDA Recall
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Maquet Getinge Group battery modules for use with Maquet SERVO-i ventilator systems (Part #6487180).... 1 04/26/2013 Maquet Cardiovascular Us Sales, Llc
Servo-i ventilator system Product Usage: Intended for treatment and monitoring of patients in th... 2 04/03/2012 Maquet Inc.
Servo-s ventilator system Product Usage: Intended for treatment and monitoring of patients in th... 2 04/03/2012 Maquet Inc.
Maquet PC Board PC1772 Spare Part Device Part number 64 67 620 Intended for treatment of and mon... 2 12/02/2011 Maquet Inc.
Maquet Servo-i ventilator system Device Part number 64 87 800 Intended for treatment of and moni... 2 12/02/2011 Maquet Inc.
Maquet Servo-S ventilator system Device Part number 66 40 440 Intended for treatment of and moni... 2 12/02/2011 Maquet Inc.
SERVO-i Ventilator System Maquet Critical Care, Solna, Sweden. The product is intended for treatme... 2 09/23/2008 MAQUET Inc.
SERVO-s Ventilator System, Maquet Critical Care, Solna, Sweden. The product is intended for treatme... 2 09/23/2008 MAQUET Inc.
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