FDAApril 24, 2019device

The LinearTM 3-4 70 cm 8 Contact Lead Kit, part number M365SC2352700 is part of a spinal cord stimulation system for prescription use only as an aid in the management of chronic intractable pain of the trunk and/or limbs. Package Contents Percutaneous Permanent Lead Kits (1) Percutaneous Lead wit...

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

The hazard

The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due to the "use by date" displayed on the label which is later than the correct "use by date". No adverse health consequence is expected to occur from this issue.

What to do

FDA enforcement status: Terminated

Brands named

boston scientific neuromodulationbostonboston scientific

Recall history

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

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