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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Latex-Free Symbiq Pump Set, convertible pin, 106 inch piggyback with backcheck valve, 2 CLAVE ports,... | 2 | 03/09/2010 | Hospira Inc. |
Primary Symbiq Set, Latex-Free, Polyethylene-Lined tubing, piggyback with backcheck valve, 2 CLAVE... | 2 | 03/09/2010 | Hospira Inc. |
LifeShield Latex-Free Primary SYMBIQ Set, Piggyback with Backcheck Valve, 3 Prepierced Y-Sites, 106 ... | 2 | 02/22/2010 | Hospira Inc. |
Hospira Phoenix Infusion System with MedNet Software, Symbiq Two-Channel Infusion System, Software v... | 2 | 08/11/2009 | Hospira Inc |
Hospira Phoenix Infusion System with MedNet Software, Symbiq One-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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