DePuy Orthopaedics, Inc.: Medical Device Recalls in 2022

According to to data from the FDA, there were 13 medical device recalls made by DePuy Orthopaedics, Inc. in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

• MODULAR CATHCART FRACTURE HEAD HIP BALL, sizes 41mm to 60mm inclusive; metallic femoral head prosthesis, Product No. 136341000, 136342000, 136343000, 136344000, 136345000, 136346000, 136347000, 136348000, 136349000, 136350000, 136351000, 136352000, 136353000, 136354000, 136356000, 136358000, 136360000
• GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610
• ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bone cuts in preparation for the femoral implant Part Number: 254400525
• GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100
• GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100
• ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001
• GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100
• GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100
• GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600
• ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154909003
• GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100
• GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600
• VELYS Robotic-Assisted Solution Base Product No.: 451570100