Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-1849-2011 - HEMOCUE AB Hb 201 DM ANALYZER, in vitro diagnostic device for quantitative hemoglobin determination. | 2 | 03/30/2011 |
FEI # 3005104838 Hemo Cue, Inc. |
| Z-1848-2011 - HEMOCUE AB GLUCOSE 201 DM ANALYZER, in vitro diagnostic device for quantitative determination of blood glucose level. | 2 | 03/30/2011 |
FEI # 3005104838 Hemo Cue, Inc. |
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