Day

December 27, 2024
27
Dec

FDA Recall: Software Issues in Updated Applications

December 27, 2024
Company: Medtronic Neuromodulation Date of Enforcement Report: 12/27/2024 Class II PRODUCT SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B Recall Number: Z-0771-2025 REASON: Software issues were identified in application version 2.x. RECALLING FIRM/MANUFACTURER: Medtronic Neuromodulation...
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