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U.S. Department of Health and Human Services

Medical Device Recalls
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61 to 70 of 500 Results *
Recall Date to: 04/08/2014
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Product Description
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FDA Recall
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COUGAR® Steerable Guidewire; Models: LVCLS190J, LVCLS190S, LVCXT190J, LVCXT190S Medtronic guide w... 1 11/15/2013 Medtronic Vascular
THUNDER® Steerable Guidewire; Model: LVTNDR190S Medtronic guide wires are steerable guide wires ... 1 11/15/2013 Medtronic Vascular
ZINGER® Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J, LVZRMS180S, LVZRXT180J, LVZ... 1 11/15/2013 Medtronic Vascular
Baylis Medical TorFlex Transseptal Guiding Sheath, Rx Only, non-pyrogenic, sterile. Product Usage... 1 11/01/2013 Baylis Medical Corp *
Edwards Lifesciences EMBOL-X Glide Protection System; Model Numbers: EXGF24D, EXGF24LLD, EXGF24MMD, ... 1 10/31/2013 Edwards Lifesciences, LLC
PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower G.I. Endoscopes are p... 1 10/28/2013 Pentax Medical Company
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT Sys... 1 10/28/2013 Atossa Genetics, Inc.
GE Healthcare, Avance, Avance CS2, Aisys, Aespire View, and Engstrom. Intended for volume or pres... 1 10/15/2013 GE Healthcare, LLC
GE Healthcare, Aisys, Amingo, Avance, and Avance CS2. Intended for volume or pressure control ven... 1 10/15/2013 GE Healthcare, LLC
Draeger Fabius GS Premium, Fabius OS, Fabius Tiro, Fabius Tiro D-M Product Usage: used to admi... 1 10/10/2013 Draeger Medical, Inc.

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