Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K022203 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Hospira LifeCare PCA3 Infusion System Software, versions 4.08 and 4.09 | 2 | 03/09/2006 | Hospira Inc |
| LifeCare PCA 3, list #s 12384-04-01, 12384-04-03, 12384-04-05, 12384-04-07, 12384-04-09, 12384-04-51... | 2 | 10/06/2009 | Hospira Inc |
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