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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
510(K) Number: K902031
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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MINOR PROCEDURE PACK 40/CS Used by medical staff to perform surgical procedures and patient care... 2 09/03/2015 FEI # 2648727
Customed, Inc
MAJOR LAPAROTOMY PK 4/CS Used by medical staff to perform surgical procedures and patient care... 2 09/03/2015 FEI # 2648727
Customed, Inc
MAJOR LAP PACK 4/CS Used by medical staff to perform surgical procedures and patient care procedur... 2 09/03/2015 FEI # 2648727
Customed, Inc
LAPAROTOMY PACK CUSTOMED 7/CS Used by medical staff to perform surgical procedures and patient ... 2 09/03/2015 FEI # 2648727
Customed, Inc
Catalog Number: 9002516 LAPAROTOMY SURGICAL PACK Used by medical staff to perform surgical proce... 2 04/14/2016 FEI # 2648727
Customed, Inc
Catalog Number: 900176 LAPAROTOMY SURGICAL PACK Used by medical staff to perform surgical procedu... 2 04/14/2016 FEI # 2648727
Customed, Inc
Catalog Number: 900052 MINOR PROCEDURE SURGICAL PACK Used by medical staff to perform surgical pr... 2 04/14/2016 FEI # 2648727
Customed, Inc
Catalog Number: 900036 LAPAROTOMY SURGICAL PACK Used by medical staff to perform surgical procedu... 2 04/14/2016 FEI # 2648727
Customed, Inc
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