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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 *
Recall Date to: 03%2F02%2F2014 Firm: DePuy
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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.
ATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee 2 04/30/2018 DePuy Orthopaedics, Inc.
Confidence Plus Kit Spinal Cement System, Product Codes: 283910000 (GTIN: (01)10705034209623) and 28... 2 04/03/2018 DePuy Spine, Inc.
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; ... 2 03/20/2018 DePuy Orthopaedics, Inc.
Concorde Lift Torque Limiting Handle. Must be used with supplemental internal spinal fixation s... 2 03/02/2018 DePuy Orthopaedics, Inc.
Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have ... 2 03/02/2018 DePuy Orthopaedics, Inc.

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