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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K902029
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Product Description
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Recall
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FDA Recall
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Catalog Number: 9001296 PREMIUM LAPAROTOMY PACK Used by medical staff to perform surgical procedu... 2 04/14/2016 Customed, Inc
Catalog Number: 900996 LAPAROTOMY SURGICAL PACK Used by medical staff to perform surgical proced... 2 04/14/2016 Customed, Inc
Catalog Number: 900547 BASIC SURGICAL PACK Used by medical staff to perform surgical procedures ... 2 04/14/2016 Customed, Inc
LAPAROTOMY BASIC PACK 10/CS Used by medical staff to perform surgical procedures and patient car... 2 09/03/2015 Customed, Inc
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