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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 10 Results
510(K) Number: K941214
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Product Description
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Recall
Class
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FDA Recall
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Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the a... 2 01/11/2017 Hospira Inc.
Lifeshield, latex-free, 150 mL Burette Set, convertible pin, 100 inch with 2 pre-pierced injection s... 2 04/15/2010 Hospira Inc.
LifeShield Latex-Free HEMA Blood PlumSet, Nonvented, 110 Inch with 210 Micron Filter, Prepierced Inj... 2 11/24/2005 Hospira Inc.
LifeShield Latex-Free HEMA Blood PlumSet; Nonvented, 100 inch, with 210 Micron Filter, Prepierced In... 2 11/15/2005 Hospira Inc.
LifeShield Latex-Free HEMA Y-Type Blood PlumSet, Nonvented, 122 inch, with 210 Micron Filter, Prepie... 2 11/15/2005 Hospira Inc.
LifeShield Latex-Free HEMA Y-Type Blood PlumSet, Nonvented, 122 inch, with 210 Micron Filter, Inline... 2 11/15/2005 Hospira Inc.
I.V. Pump Sets with Cassettes for use with Abbott Plum Series and Lifecare Infusion Pumps; sterile, ... 2 06/27/2003 Abbott Laboratories HPD/ADD
Vented and Non-Vented Burette I.V. Gravity Feed Administration Sets; sterile, Rx, single use devices... 2 06/27/2003 Abbott Laboratories HPD/ADD
I.V. Extension Sets; sterile, Rx, single use devices; Abbott Laboratories, North Chicago, IL 60064 U... 2 06/27/2003 Abbott Laboratories HPD/ADD
Abbott Latex-Free Primary I.V. Plumset Convertible Pin, 95 inch with Injection Site and Secure Lock,... 2 06/17/2003 Abbott Laboratories HPD/ADD
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