Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K830014 |
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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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| LifeShield Latex-Free Primary I.V. Pump Set with Distal Microbore Patient Line and Gravity Flow Prev... | 2 | 02/27/2007 |
FEI # 3013319212 Hospira Inc. |
| Hospira Latex Free Blood Secondary Set, 26 inch with Secure Lock; Made in Costa Rica, Hospira, Inc.,... | 2 | 02/08/2006 |
FEI # 3013319212 Hospira Inc. |
| LifeShield Latex-Free HEMA Blood PlumSet, Nonvented, 110 Inch with 210 Micron Filter, Prepierced Inj... | 2 | 11/24/2005 |
FEI # 3013319212 Hospira Inc. |
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