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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K883320
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Product Description
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FDA Recall
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MONOJECT Blood Collection Tubes containing heparin 13x100 sodium heparin trace element Item Code 8... 2 03/07/2011 FEI # 1282497
Covidien LP
MONOJECT Blood Collection Tubes containing heparin 10x64 Sodium Heparin Item code 8881320256 2 03/07/2011 FEI # 1282497
Covidien LP
MONOJECT Blood Collection Tubes containing heparin 10x50 Sodium Heparin Item code 8881320157 2 03/07/2011 FEI # 1282497
Covidien LP
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