Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K041444 |
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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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D-10 Dual Program Reorder Pack; contains 400 HbA1c or 200 HbA2/F/A1c tests. Kits include Elution Bu... | 3 | 07/27/2011 | Bio-Rad Laboratories Inc |
Bio-Rad D-10 Dual Program Calibrator Diluent, a component of the Bio-Rad D10 Dual Program diagnostic... | 2 | 01/25/2007 | Bio-Rad Laboratories Inc |
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