Z-2122-2020 Class II Terminated

Recalled by Boston Scientific Neuromodulation Corporation — Valencia, CA

Recall Details

Product Type
Devices
Report Date
June 3, 2020
Initiation Date
April 24, 2019
Termination Date
January 18, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1 unit

Product Description

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

Reason for Recall

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.

Distribution Pattern

Distributed OUS only. to 14 countries.

Code Information

Part number M365SC2352700; serial number 1042757.