Implant Direct Sybron Manufacturing, LLC: Medical Device Recall in 2017 - (Recall #: Z-2125-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD

Product Classification:

Class II

Date Initiated: May 2, 2017

Date Posted: May 31, 2017

Recall Number: Z-2125-2017

Event ID: 77171

Reason for Recall:

Implant Direct Sybron Manufacturing is recalling the Legacy Full-Contour Abutment 3.5mmD Assembly because it may be out of Implant Direct specification.

Status: Terminated

Product Quantity: 151 units

Code Information:

89103, 83493, 78986

Distribution Pattern:

Worldwide Distribution - Nationwide Distribution and to the countries of : European Union (HU, GB, DE, DK, IT, HR, FR), and Japan

Voluntary or Mandated:

Voluntary: Firm initiated