Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K021023 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 | 2 | 12/16/2013 | Instrumentation Laboratory Co. |
HemosIL High Abnormal Control 3 UNASSAYED Part Number: 0020003320 | 2 | 12/16/2013 | Instrumentation Laboratory Co. |
HemosIL Low Abnormal Control 2 UNASSAYED Part Number: 0020003220 | 2 | 12/16/2013 | Instrumentation Laboratory Co. |
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