Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K020935 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| HemoCue® Glucose 201 Microcuvettes, The HemoCue Glucose 201 Microcuvettes are designed for use with ... | 2 | 12/24/2014 |
FEI # 1523456 Radiometer America Inc |
| The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose 201 (or DM) Anal... | 2 | 07/02/2025 |
FEI # 3003044483 HemoCue AB |
| HemoCue® Glucose 201 Microcuvettes, 25 Microcuvettes Individually Packaged. The HemoCue Glucose... | 2 | 09/11/2013 |
FEI # 3003044483 HemoCue AB |
| HemoCue Glucose 201 Microcuvettes, Article Number:110705*,110706,110715**,110716**,110717**,1107... | 3 | 01/20/2012 |
FEI # 3005104838 Hemo Cue, Inc. |
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