Implant Direct Sybron Manufacturing, LLC: Medical Device Recalls in 2018

According to to data from the FDA, there were 8 medical device recalls made by Implant Direct Sybron Manufacturing, LLC in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

• Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile, 3.5mmD Platform. Dental implant component, used temporarily during impressions for the prosthetic procedure.
• REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60
• Implant Direct, INTERACTIVE HEALING COLLAR, PART NUMBER 6530-15, 5.0mmL: 3.0mmD Platform
• ImplantDirect Legacy 4 Implant, 5.7mmD x 5.7mmD Platform, Part 885708, Rx, Sterile. The incorrect cap label shows part 855708, 5.7mmD Platform, 8mmL.
• SwishTapered Implant Intended for use in support for fixed bridgework.
• ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U, Rx, Sterile. Incorrect label on the cap says 4.3mmD Platform 604313U 13mmL. Product Usage: Usage: Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit restorations and terminal or intermediate abutment support for fixed bridgework.
• SwishPlus Implant Intended for use in support for fixed bridgework.
• ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit restorations and terminal or intermediate abutment support for fixed bridgework.