PlainRecalls
FDA Devices Moderate Class II Ongoing

SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D

Reported: January 8, 2025 Initiated: November 21, 2024 #Z-0773-2025

Product Description

SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D

Reason for Recall

Software issues were identified in application version 2.x.

Details

Recalling Firm
Medtronic Neuromodulation
Units Affected
566 systems
Distribution
Worldwide - US Nationwide distribution.
Location
Minneapolis, MN

Frequently Asked Questions

What product was recalled?
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D. Recalled by Medtronic Neuromodulation. Units affected: 566 systems.
Why was this product recalled?
Software issues were identified in application version 2.x.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 8, 2025. Severity: Moderate. Recall number: Z-0773-2025.