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Tornier, Inc recalls Ratcheting Screwdriver Handle, provided in the Aequalis Perform Reversed kit
Recalled June 8, 2022 · FDA recall Z-1216-2022 · Tornier
Hazard
The device is unable to meet sterilization requirements when sterilized per instructions in an Aesculap container. · FDA Class II
Units
1066 units
Sold at
US Nationwide distribution.
Description
The device is unable to meet sterilization requirements when sterilized per instructions in an Aesculap container.
Product
Ratcheting Screwdriver Handle, provided in the Aequalis Perform Reversed kit
Manufacturer(s)
Tornier, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →