Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K883320 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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