FDAJanuary 11, 2016device

Specify 5-6-5 Lead, Specify 2x8 Lead, Model Numbers: 39565, 39286. Spinal cord stimulation leads. Part of a neurostimulation system for treating chronic, intractable pain of the trunk and/or limbs-including unilateral or bilateral pain.

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

The hazard

Some Specify 5-6-5 and 2x8 surgical lead product labeling does not adequately distinguish between permanent surgical implant and trialing/screening use.

What to do

FDA enforcement status: Terminated

Brands named

medtronic neuromodulationmedtronic

Recall history

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

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Specify 5-6-5 Lead, Specify 2x8 Lead, Model Numbers: 39565, 39286. Spinal cord stimulation leads. Part of a neurostimulation system for treating chronic, intractable pain of the trunk and/or limbs-including unilateral or bilateral pain. — Recall Details · AllClear