Implant Direct Sybron Manufacturing LLC: Device Recall

Recall #Z-2172-2025 · 05/01/2025

Class II: Risk

Recall Details

Recall Number
Z-2172-2025
Classification
Class II
Product Type
Device
Recalling Firm
Implant Direct Sybron Manufacturing LLC
Status
Ongoing
Date Initiated
05/01/2025
Location
Westlake Village, CA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
45 Kits

Reason for Recall

The Drill stop kit contains incorrect components.

Product Description

The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop length, and facilitate the mounting/removal of the Drill Stops. The Drill Stop Kit includes the Release Bracket, which is used for mounting and removing Drill Stops, as well as verifying the length of the Drill Stops via a ruler and depth markings. The Drill Stop Kit also allows for optional storage of some DLC drills. Drill Stops: The Drill Stop is a reusable (up to 30 osteotomies) hollow cylinder with retention prongs that clips onto the hub of the DLC drill, creating a stop function at the desired predetermined drill depth (6mm, 8mm, 10mm, 11.5mm, 13mm and 16mm). The Drill Stops come in two formats (Short  6-13mm depth, and Long  6-16mm depth), and in several diameters for different diameter drills.

Distribution Pattern

Worldwide - US Nationwide distribution in the states of AL, FL, LA, MD, NJ, NV, NY, OH, OK, TN, TX, UT, VA and the country of Japan.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.