FDAApril 24, 2019device

Precision TM M8 Adapter, 15 cm, part number M365SC9218150 - Product Usage: The adapter is part of a spinal cord stimulation system for prescription use only indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs including unilateral or bilateral pain associate...

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 "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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