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