Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K950419 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Alaris Pump Module, Model 8100. | 1 | 08/03/2009 |
FEI # 2016493 Cardinal Health 303 dba Cardinal Health |
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