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Recall Observatory FDA recall evidence

Device product

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 with pre-loaded Curved Stylet (1) Stylet Ring with a Curved and a Straight Stylet (4) Suture Sleeves (1) Insertion Needle with Stylet (1) Lead Blank (1) Steering Cap (1) OR Cable Assembly (2) Lead Position Labelsleft and right (non-sterile) (1) Device Registration Form/Temporary Patient Identification Card (1) Manual

Z-2122-2020

April 24, 2019

Class II

Product summary

Firm
Boston Scientific Neuromodulation Corporation
Event
Event 84983
Status
Terminated
Classification
Class II
Quantity
1 unit
Official record key
device-enforcement:Z-2122-2020

Official wording

Reason: 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.

Code information: Part number M365SC2352700; serial number 1042757.

Distribution pattern: Distributed OUS only. to 14 countries.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.