DePuy Orthopaedics, Inc.: 94 recalls on record

Recalls filed with 1 agency: FDA (94).

First recall on record: July 11, 2012. Most recent: April 10, 2024.

Risk classification: Class I: 5 · Class II: 88 · Class III: 1

Most recent recalls

DateAgencyProduct
April 10, 2024FDAATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Component of t…Z-1456-2024
March 29, 2023FDAAttune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM, Part Number 1517603…Z-1266-2023
March 29, 2023FDAAttune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM, Part Number 151760…Z-1264-2023
July 27, 2022FDAATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bon…Z-1419-2022
February 16, 2022FDAATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total kn…Z-0631-2022
January 19, 2022FDAGLOBAL UNITE REV STEM SZ 10 Product Code: 110010600Z-0487-2022
January 19, 2022FDAGLOBAL UNITE STD STEM SZ 16 Product Code: 110016100Z-0490-2022
February 19, 2020FDASPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The product is a femoral …Z-1169-2020
September 5, 2018FDAP.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830Z-2949-2018
May 16, 2018FDAATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Imp…Z-1704-2018
April 4, 2018FDA(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603…Z-1219-2018
March 7, 2018FDADELTA XTEND" Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants in…Z-0834-2018
June 14, 2017FDADePuy Synthes various orthopedic instruments modified by U.S. Distributors These instr…Z-2317-2017
December 24, 2014FDACeramic Femoral Head. Intended for use in total hip arthroplasty applications to rep…Z-0825-2015
November 19, 2014FDAATTUNE Intuition Distal Femoral Jig; sold non-sterile; product is wrapped in bubble wrap …Z-0199-2015
October 15, 2014FDARECLAIM Distal Reamer Extension Non Sterile REF 2975-00-500 Intended as an attachme…Z-0038-2015
October 15, 2014FDACharnley PN Retract & Handle, REF 962004000, Non-Sterile-DuPuy International Ltd. The …Z-0061-2015
July 30, 2014FDARECLAIM DISTAL TAPERED, Angled Distal Stem, various sizes. Taper Protector Sleeve. RECLA…Z-2083-2014
July 30, 2014FDARECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical I…Z-2082-2014
July 30, 2014FDARECLAIM DISTAL TAPERED Distal Stem, various sizes. Taper Protector Sleeve. RECLAIM Revis…Z-2084-2014
April 16, 2014FDAGLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Part # 2230-00-019, No…Z-1437-2014
March 19, 2014FDAREF 623421 RS-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Righ…Z-1208-2014
March 19, 2014FDAREF 623401 L S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Le…Z-1203-2014
March 19, 2014FDAREF 623421 L S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Lef…Z-1207-2014
March 19, 2014FDAREF 623411 L, S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Le…Z-1205-2014

Questions about this company

How many recalls does DePuy Orthopaedics, Inc. have?
Recalert has 94 U.S. recalls on record for DePuy Orthopaedics, Inc., published between July 11, 2012 and April 10, 2024.
What was the most recent DePuy Orthopaedics, Inc. recall?
FDA recall Z-1456-2024, published April 10, 2024: ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Component of the ATTUNE Total Knee Replacement System.
Which agencies have handled DePuy Orthopaedics, Inc. recalls?
DePuy Orthopaedics, Inc. appears as the recalling firm in recalls from: FDA (94).

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