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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 *
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Product Description
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FDA Recall
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Panta® Arthrodesis Nail Support device, 510 (k) #K050882. One (1) unit of product is kitted within ... 2 04/16/2012 FEI # 3003418325
Integra LifeSciences Corp.
Part Number 496311, Lot Number 99768100 Multi-purpose Kit blister tray coupled with Tyvek lid st... 2 04/27/2011 FEI # 1625425
Argon Medical Devices, Inc
Peak Vest, Single Item, Product Number PVest, Part Numbers REPVEST*M, SEPVESTE, SEPVEST*F Produc... 2 07/30/2019 FEI # 1000120804
Burlington Medical, LLC
Persona Stemmed 5 Degree Cemented Tibia Product Usage: This device is indicated for patients ... 2 11/08/2014 FEI # 1000220733
Zimmer, Inc.
Philips Medical System Extended Brilliance Workspace (EBW), Computed Tomography X-Ray System. T... 2 03/05/2013 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
Platen, Catalog # 301-124, is a mechanism used to lock or hold the fill tube in place as it is fill... 3 04/06/2005 FEI # 3003179719
The Spineology Group
Podiatry Pack - contains Devon Light Glove Used during surgery 2 07/07/2015 FEI # 1000111025
Stradis Healthcare, LLC.
Polymeric coated stent. Cypher BX Velocity Cardio Sirolimus Stents. 2 01/26/2005 FEI # 1016427
Cordis Corporation
Product Brand Name: Versafitcup Double Mobility Liner Inserter Product Generic Name: Versafitcup ... 2 06/30/2011 FEI # 3006639916
Medacta Usa Inc
Product is labeled in part: "***REF: 01-7036, LOT 999999, "1.5MM" SYSTEM PLATE L-SHAPE, 3 X 3 HOL... 2 03/23/2012 FEI # 1032347
Biomet Microfixation, LLC

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