Synthes, Inc.: Medical Device Recall in 2020 - (Recall #: Z-2698-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

MatrixNEURO Screws - Product Usage: The intended use for this device is in fixation of cranial bones and facial skeleton in procedures such as craniotomies, reconstructive procedures, fracture repair, osteotomies, and selective orthognathic surgery of the maxilla and chin.

Product Classification:

Class II

Date Initiated: June 18, 2020

Date Posted: August 5, 2020

Recall Number: Z-2698-2020

Event ID: 85899

Reason for Recall:

One lot of MatrixNEURO 5mm screws was packaged in a body clip etched "4", which indicated a 4mm screw. The outer package labeling correctly identifies a 5mm screw, but the body clop incorrectly identifies a shorter length for the screw.

Status: Terminated

Product Quantity: 104 units

Code Information:

Lot # 30P6198

Distribution Pattern:

International distribution including in the countries of Australia, Belgium, Chile, France, Slovakia, South Korea.

Voluntary or Mandated:

Voluntary: Firm initiated