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U.S. Department of Health and Human Services

Medical Device Recalls
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191 to 200 of 500 Results *
Recall Date to: 07/31/2015
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Product Description
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FDA Recall
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Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: The SofPort/SoFlex IOLs are int... 2 07/20/2015 Bausch & Lomb Surgical, Inc.
GE Healthcare Precision 500D Classical R & F system. 2 07/20/2015 GE Healthcare
GE Healthcare, Precision MPi fluoroscopic imaging systems. 2 07/20/2015 GE Healthcare
GE Healthcare Precision RXi Digital system 2 07/20/2015 GE Healthcare
GE Healthcare Precision RXi 23A/32A Analog System 2 07/20/2015 GE Healthcare
Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per... 1 07/20/2015 Western / Scott Fetzer Company
Cochlear Nucleus Sterile Silicone Template Product Usage: The Cochlear Nucleus Sterile Silicone... 2 07/20/2015 Cochlear Americas Inc.
Polaris 4.75 TI Spinal System, 4.0 x 20 MM, Closed MAS, Closed Head Multiaxial Screw, Non-Sterile, R... 2 07/20/2015 Biomet Spine, LLC
NS-3600-B LITE GLOVE 1000/CASE -Bulk, Non-sterile Catalog Number: 571711 2 07/20/2015 Covidien LLC
Non Sterile Subassembly: Catalog Number/Description: SA1008 NONSTERILE SUBASSEMBLY SA1578 NO-STE... 2 07/20/2015 Covidien LLC

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