FDAApril 26, 2016device

Torque Limiting Handle: PRECIMED, T-Handle Torque, Non Sterile. Handle: Customer Number/Model: MCL120014 T14000, TLT911-50-S20 TLT911-50-S20, TLT911-15-S01 TLT911-15-S01, TLTS0007-20-S19 TLTS0007-20-S19, TLT911-35-S01 TLT911-35-S01.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Greatbatch Medical has initiated a global Field Recall for Torque Limiting Devices. Greatbatch identified through laboratory testing that the required sterility assurance level (SAL) of 10-6 is not achieved on torque limiting devices when subjected to steam sterilization cycles identified in the Instruction For Use (IFU) provided with the device.

What to do

FDA enforcement status: Terminated

Brands named

greatbatch medicalgreatbatch

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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