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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 23 Results
510(K) Number: K051499
 
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Product Description
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Class
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FDA Recall
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Medrad(R) Continuum MR Infusion System Standard Administration Kit Peristaltic Pump System design... 2 12/20/2012 Medrad Inc
Medrad(R) Continuum MR Infusion System Secondary Administration Kit Peristaltic Pump System desig... 2 12/20/2012 Medrad Inc
Medrad(R) Continuum MR Infusion System Primary Set Peristaltic Pump System designed for patients ... 2 12/20/2012 Medrad Inc
Medrad(R) Continuum MR Infusion System Primary VSA Stopcock Set Peristaltic Pump System designed ... 2 12/20/2012 Medrad Inc
Medrad(R) Continuum MR Infusion System Primary VSA Set Peristaltic Pump System designed for patie... 2 12/20/2012 Medrad Inc
Medrad(R) Continuum MR Infusion System Primary Spike Set Peristaltic Pump System designed for pat... 2 12/20/2012 Medrad Inc
Medrad(R) Continuum MR Infusion System Secondary Set Peristaltic Pump System designed for patient... 2 12/20/2012 Medrad Inc
Medrad(R) Continuum MR Infusion System Secondary Spike Set Peristaltic Pump System designed for p... 2 12/20/2012 Medrad Inc
Medrad(R) Continuum MR Infusion System Secondary VSA Set Peristaltic Pump System designed for pat... 2 12/20/2012 Medrad Inc
Medrad(R) Continuum MR Infusion System Side Step Set Peristaltic Pump System designed for patient... 2 12/20/2012 Medrad Inc
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