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U.S. Department of Health and Human Services

Medical Device Recalls
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101 to 110 of 500 Results *
Recall Date to: 04/19/2015
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Integra® Flowable Wound Matrix Size 3cc 1 unit/box single use, sterile device Rx Only Model Num... 2 04/16/2015 Integra LifeSciences Corp.
Magellan Robotic System; Model No(s). 11132 and 11139. A steerable catheter control system used at ... 2 04/15/2015 Hansen Medical Inc
SpermMar Test 0.7ml Beads Particles Label on bottle: SpermMar Test IgA 0.7ml Beads/Particles-5... 2 04/15/2015 Vitrolife Inc
Bard Monopty Disposable Core Biopsy Instruments and Kits, Monopty 14g x 16cm (22mm), Product Code: 1... 2 04/14/2015 Bard Peripheral Vascular Inc
Artis Q/ Q zen systems; Artis Q/ Q zen systems are dedicated angiography systems developed for singl... 2 04/14/2015 Siemens Medical Solutions USA, Inc
LOW PROFILE NON-LOCK SCREW; 2.7mm x 22 mm; REF 131227222; LOT RM105E. Provides the orthopaedic s... 2 04/14/2015 Biomet, Inc.
Hardy Diagnostics cat no. G327 HardyCHROM SS Agar (HardyCHROM Salmonella Shigella) Cat no: G327... 2 04/14/2015 Hardy Diagnostics
Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter kits containing Safe-Cut Sa... 2 04/14/2015 Bard Access Systems
Kenex Radiation Shield installed with GE Healthcare Interventional, Surgery, CT and X-Ray Imaging sy... 2 04/13/2015 GE Healthcare
ProTrack Microcatheter; Product Usage: The ProTrack Microcatheter is a sterile, single use devi... 2 04/13/2015 Baylis Medical Corp *

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