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U.S. Department of Health and Human Services

Medical Device Recalls

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81 to 90 of 500 Results *
Product: nti
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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1.5T Signa HDxt, 3.0T Signa HDxt, Signa HDi, Signa Vibrant Product Usage: The 1.5T Signa HDx fa... 2 08/02/2017 GE Medical Systems, LLC
10% Buffered Formalin Phosphate; Certified For laboratory and manufacturing use only, not for drug,... 2 08/25/2008 ThermoFisher Scientific Co., LLC
10) Brivo MR355/Optima MR360 Not yet 510(K) cleared and are not distributed in the US. (K103330) ... 2 02/24/2011 GE Healthcare, LLC
100 ft roll of tubing inside a cardboard box. Medical devices are sealed into the tubes prior to eth... 3 09/06/2012 Steris Corporation
100-120V 2001 Pulse Oximeter With Mars - Dixtal owned product. Intended use is to provide continu... 2 04/08/2010 Philips Healthcare Inc.
100-120V 2001 Pulse Oximeter with Mars Nurse Call - Dixtal owned product. Intended use is to prov... 2 04/08/2010 Philips Healthcare Inc.
100-120V 2001 Pulse Oximeter with Mars Nurse Call, Refurbished - Dixtal owned product. Intended u... 2 04/08/2010 Philips Healthcare Inc.
100-120V 2001 Pulse Oximeter with Mars, Refurbished - Dixtal owned product. Intended use is to pr... 2 04/08/2010 Philips Healthcare Inc.
100-120V 515B with RS-232 Pulse Oximeter - Dixtal owned product. Intended use is to provide conti... 2 04/08/2010 Philips Healthcare Inc.
100-120V Capnogard 1265, Refurbished, Respironics/Philips product. Intended to be used for monito... 2 04/08/2010 Philips Healthcare Inc.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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