FDA recall Z-0185-2018

Implant Direct Sybron Manufacturing, LLC · Class II · device

Product

ImplantDirect Legacy(TM) 3 Implant, 13MM L, REF 864713 This Legacy implant is a two-piece implant for one-stage or two-stage surgical procedures. These implants are 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.

Reason for recall

One reported complaint and discovered that the outer vial was out of round and undersized. Therefore a portion of the opening may not allow inner vial and components to slide freely out of the vial. As a result, the cap could possibly not be screwed on properly and the sterilization compromised.

Distribution

Worldwide distribution: US (nationwide) including Puerto Rico and country of Japan.

Key facts

Status
Terminated
Initiation date
2017-10-10
Report date
2017-12-06
Termination date
2018-09-27
Voluntary/Mandated
Voluntary: Firm initiated
Location
Westlake Village, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0185-2018