Boston Scientific Neuromodulation Corporation Recall: Thirty-five (35) cm 8 Contact Extens
Boston Scientific Neuromodulation Corporation Recall: Thirty-five (35) cm 8 Contact Extens is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Boston Scientific Neuromodulation Corporation; Product: Thirty-five (35) cm 8 Contact Extension Kit, part number M365SC3138350. Package Contents: L
| Recalling firm | Boston Scientific Neuromodulation Corporation |
|---|---|
| Product | Thirty-five (35) cm 8 Contact Extension Kit, part number M365SC3138350. Package Contents: Lead Extension Kit (1) Lead Extension (1) Hex Wrench (1) Tunneling Tool Assembly (1) Device Registration Form/Temporary Patient Identification Card (1) Manual Product Usage: Contact extension kits are 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. They are designed to connect the percutaneous leads to the Implantable Pulse Generator (IPG) for spinal cord stimulation. |
| 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. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Distributed OUS only. to 14 countries. |
| Recall initiated | 20190424 |
| Recall number | Z-2120-2020 |
| Category | device |
| State | CA |
| Country | United States |
$29/mo
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