Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K031043 |
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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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Bio Rad brand D-10 Hemoglobin A1c Program Reorder Pack, which contains Update Kit D-10 A1c Program D... | 3 | 04/13/2011 | Bio-Rad Laboratories, Inc., Hercules, CA |
D-10" Hemoglobin Testing System, Model number: 220-0220 Manufactured by: Bio-Rad Laboratories,... | 2 | 03/27/2014 | Bio-Rad Laboratories, Inc. |
D-10 Dual Program, which contains Update Kit D-10 A1c program diskette. United States; Bio-Rad La... | 3 | 02/10/2014 | Bio-Rad Laboratories, Inc. |
D-10 Hemoglobin A1c Program Elution Buffer 2: Bio-Rad Laboratories, Hercules, CA 94547. Perce... | 3 | 10/07/2011 | Bio-Rad Laboratories, Inc. |
D-10 Hemoglobin A1c Program Reorder Pack; 400 tests; For the determination of Hemoglobin A1c in hum... | 3 | 10/07/2011 | Bio-Rad Laboratories, Inc. |
D-10 Hemoglobin A1c Supplemental Reagent Pack: Bio-Rad Laboratories, Hercules, CA 94547. Perc... | 3 | 10/07/2011 | Bio-Rad Laboratories, Inc. |
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