FDAApril 24, 2017device

Response BandLoc 5.5/6.0 Tensioner Instrument The Tensioner Instrument (01-1102-1000) is utilized to allow the surgeon to apply a recommended tension to the band and hold it in place during spine manipulation and set screw tightening.

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

The hazard

Over-tensioning of the band resulting in damage to the band causing it to rupture

What to do

FDA enforcement status: Terminated

Brands named

orthopediatrics

Recall history

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

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Response BandLoc 5.5/6.0 Tensioner Instrument The Tensioner Instrument (01-1102-1000) is utilized to allow the surgeon to apply a recommended tension to the band and hold it in place during spine manipulation and set screw tightening. — Recall Details · AllClear