Tornier, Inc: Medical Device Recall in 2022 - (Recall #: Z-1216-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Ratcheting Screwdriver Handle, provided in the Aequalis Perform Reversed kit

Product Classification:

Class II

Date Initiated: May 3, 2022

Date Posted: June 8, 2022

Recall Number: Z-1216-2022

Event ID: 90052

Reason for Recall:

The device is unable to meet sterilization requirements when sterilized per instructions in an Aesculap container.

Status: Ongoing

Product Quantity: 1066 units

Code Information:

Model: MWJ128, Ratcheting Screwdriver Handle, all lot codes

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated