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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: 11/24/2015
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Product Description
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FDA Recall
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Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver tips are attached to a surgical drill... 2 11/12/2015 Biomet 3i, LLC
Ventilator Tubing 2 11/12/2015 Instrumentation Industries Inc
Biomet 3i Narrow Right Angle Square Driver Tip. Driver tips are attached to a surgical drilling uni... 2 11/12/2015 Biomet 3i, LLC
MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis. 2 11/12/2015 Siemens Medical Solutions USA, Inc
Medtronic Perfusion Tubing Packs, Models TL7M64R3, TL7P17R1 & HY2W85R9, Sterilized using Ethylene ... 2 11/12/2015 Medtronic Perfusion Systems
Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional suppo... 2 11/12/2015 Stryker Spine
Philips DigitalDiagnost Release 4.0.3, Release 4.1/4.1.1. excluding systems with SP1 Product Us... 2 11/11/2015 Philips Electronics North America Corporation
Boston Scientific, WATCHMAN Left Atrial Appendage Closure Device with Delivery System, 21mm x 12F ( ... 2 11/11/2015 Boston Scientific Corporation
Boston Scientific, WATCHMAN Access System Access Sheath with Dilator, 14F Single curve( M635TU1006... 2 11/11/2015 Boston Scientific Corporation
Disposable Reflective Marker Spheres The Disposable Reflective Marker Spheres used in conjunction... 2 11/11/2015 Brainlab AG

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