Medical Device Recalls
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31 to 36 of 36 Results
510(K) Number: K041550 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Hospira Inc. Symbiq One- and Two- Channel Infuser, List Numbers 16026 and 16027 respectively. | 1 | 09/08/2010 | Hospira Inc |
Hospira brand Symbiq One-Channel Infuser; List Number: 16026; Distributed by: Hospira, Inc. Morgan H... | 1 | 07/02/2010 | Hospira Inc |
Hospira brand Symbiq Two-Channel Infuser; List Number: 16027; Distributed by: Hospira, Inc. Morgan ... | 1 | 07/02/2010 | Hospira Inc |
Hospira Phoenix Infusion System with MedNet Software, Symbiq One-Channel Infusion System, Software v... | 2 | 08/11/2009 | Hospira Inc |
Hospira Phoenix Infusion System with MedNet Software, Symbiq Two-Channel Infusion System, Software v... | 2 | 08/11/2009 | Hospira Inc |
Symbiq One-Channel list number 16026-04 and Two-Channel list number 16027-04 Infusion System, a gene... | 2 | 02/27/2009 | Hospira Inc |
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