Howmedica Osteonics Corp.: Medical Device Recalls in 2022

According to to data from the FDA, there were 12 medical device recalls made by Howmedica Osteonics Corp. in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

• Tobra Full Dose CE Antibiotic Simplex P- Indicated for the fixation of prostheses to living bone in orthopaedic Catalog Number:6197-1-001
• Full Dose CE Simplex P Single Bone Cement - Indicated for the fixation of prostheses to living bone in orthopaedic Catalog Number: 6191-0-001
• Triathlon Tritanium Tibial Component (Size 6); Catalog Number 5536-B-600 Triathlon¿ Tritanium¿ Tibial Component (Size 5); Catalog Number 5536-B-500
• Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for sterilization of re-usable instruments required for implanting the Triathlon Globalization Implant System for individual patients receiving primary total knee arthroplasty (TKA). Catalog# 6541-9-109
• Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032
• 32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
• Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
• Short tibial bearing MK4 - Std, STM, Catalog No. SMMLTB02. Knee prosthesis component.
• Dall Miles SM GRIP AND 2 1.6MM HOMOG CBL, Catalog Number 6704-0-110
• Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044
• Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232
• Simplex HV With Gentamicin CE, 10 PACK-Bone cement with Gentomycin Catalog Number: 6193-1-010