Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K041874 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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ABL 800 FLEX series blood gas analyzers containing software version 5.24. | 3 | 07/24/2007 | Radiometer America Inc |
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