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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 34 Results
510(K) Number: K990899
 
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Product Description
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FDA Recall
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Alere Blood Collection Kit (Consumer Life Insurance), Product K6700, each kit packed in a bag or en... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
Appraise A1C (Retail) Collection Kit, Product K7050, each kit packed in a bag or envelope and conta... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
Appraise A1C Test Pak Kit (Alere), Product K7300, each kit packed in a bag or envelope and contains... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
Appraise A1C Test Pak Kit (Carolina Care Plan), Product K7400, each kit packed in a bag or envelope... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
Appraise A1C Test Pak Kit (Consumers Life Insurance Company), Product K7100, each kit packed in a b... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
Appraise A1C Test Pak Kit (IBM Care Advantage), Product K7200, each kit packed in a bag or envelope... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
Appraise A1C Test Pak Kit (Medical Mutual of Ohio), Product K7000, each kit packed in a bag or enve... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
Appraise A1c Retail Kit, Product K7615, each kit packed in a box and contains 1 Triad Medium Alcohol... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
Appraise DBS Kit, Product K4002, each kit packed in a bag or envelope and contains 1 Triad Medium A... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
Appraise DBS Kit, Product K8302, each kit packed in a bag or envelope. (This kit was previously Pro... 2 01/11/2012 FEI # 1000118383
Heritage Labs International LLC
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