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U.S. Department of Health and Human Services

Medical Device Recalls
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51 to 60 of 500 Results *
Firm: DePuy
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Product Description
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Concorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (19... 2 04/27/2019 DePuy Spine, Inc.
Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (... 2 04/27/2019 DePuy Spine, Inc.
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORA... 2 04/11/2019 DePuy Orthopaedics, Inc.
CORAIL AMT COXA VARA NECK SEGMENT (KLA) Pro. Code L20432 Product Usage: The affected CORAIL Neck... 2 04/11/2019 DePuy Orthopaedics, Inc.
CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO), Pro. Code L20433 Product Usage: The affected CORAIL N... 2 04/11/2019 DePuy Orthopaedics, Inc.
Mitek Screw and Washer Depth Gauge, Product Code 219024 2 10/23/2018 DePuy Mitek, Inc., a Johnson & Johnson Co.
CORAIL Cementless Femoral Stem HA Coated Standard Size 11, Catalog No. 3L92511 2 10/11/2018 DePuy Orthopaedics, Inc.
P.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830 2 08/29/2018 DePuy Orthopaedics, Inc.
LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Sho... 2 05/08/2018 DePuy Mitek, Inc., a Johnson & Johnson Co.
ATTUNE Revision CRS Femoral LT SZ 5 Cemented, Catalog No. 150440105, Femoral Revision Implant, Knee 2 04/30/2018 DePuy Orthopaedics, Inc.

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