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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-0771-2025 - 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 2 12/27/2024 FEI # 2182207
Medtronic Neuromodulation
Z-0774-2025 - SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CLINICIAN TABLET GLBL SMSNG and PROG CT900E CLINICIAN TABLET PAPER EN with the A810 CP app version 2.x, C... 2 12/27/2024 FEI # 2182207
Medtronic Neuromodulation
Z-0773-2025 - 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 2 12/27/2024 FEI # 2182207
Medtronic Neuromodulation
Z-0772-2025 - SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C 2 12/27/2024 FEI # 2182207
Medtronic Neuromodulation
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