FDAJuly 7, 2015device

S4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal System clamping screws with a defined torque 2.8 Nm for tightening the clamping screw in the screw head/hook head/occipital plate/transverse connector and other connectors.

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

The hazard

A FW103R torque wrench that was improperly reassembled after reprocessing caused a screw to break during implantation due to too much torque. The firm did not include instructions for reassembly after reprocessing.

What to do

FDA enforcement status: Terminated

Brands named

aesculap

Recall history

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

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