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  • Device 178
  • Manufacturer 0
  • Event 162
  • Implant 50
SynchroMed Implantable Infusion Pump
  • Model / Serial
  • Product Description
    AIMDD
  • Manufacturer
    Medtronic Inc.
  • 1 Event
    • Field Safety Notices about SynchroMed Implantable Infusion Pump
SYNCHROMED II Implantable Pump
  • Model / Serial
    8637-20 and 8637-40, specific serials.
  • Product Description
    To perform chronic infusion of drugs or liquids.
  • Manufacturer
    Medtronic Inc || Medtronic Neuromodulation || Medtronic Puerto Rico, Operations Co. || Medtronic Puerto Rico Operations Co., Villalba.
  • 2 Events
    • Safety Alert for SYNCHROMED II Implantable Pump
    • Safety Alert for SYNCHROMED II Implantable Pump
Implantable Pump SYNCHROMED II
  • Model / Serial
    8637-20 and 8637-40, specific serials.
  • Product Description
    To perform chronic infusion of drugs or liquids.
  • Manufacturer
    Medtronic Inc || Medtronic Neuromodulation || Medtronic Puerto Rico, Operations Co. || Medtronic Puerto Rico Operations Co., Villalba.
  • 1 Event
    • Safety Alert for Implantable Pump SYNCHROMED II
Implantable Pump SYNCHROMED II
  • Model / Serial
  • Product Description
    To perform chronic infusion of drugs or liquids.
  • Manufacturer
    Medtronic Inc || Medtronic Neuromodulation || Medtronic Puerto Rico, Operations Co. || Medtronic Puerto Rico Operations Co., Villalba.
  • 1 Event
    • Safety Alert for Implantable Pump SYNCHROMED II
Synchromed II pump
  • Model / Serial
  • Product Description
    Programmed implantable infusion pump
  • Manufacturer
    Japan Medtronic Co., Ltd.
  • 1 Event
    • Recall of Synchromed II pump
Medtronic SynchroMed II Infusion Pump
  • Model / Serial
    Model: SynchroMed II, Affected: All serial numbers
  • Product Classification
    General Hospital and Personal Use Devices
  • Manufacturer
    Medtronic Inc
  • 1 Event
    • Recall of Medtronic SynchroMed II Infusion Pump
SynchroMed EL Drug Infusion Pump
  • Model / Serial
    Model: Models 8627-10, 8627L-10, 8627-18, 8627L-18 /CN, Affected: All serial numbers
  • Product Classification
    General Hospital and Personal Use Devices
  • Manufacturer
    Medtronic Inc
  • 1 Event
    • Recall of SynchroMed EL Drug Infusion Pump
Medtronic Synchromed II Implantable Infusion Pump
  • Model / Serial
    Model: , Affected: All serial numbers
  • Product Classification
    General Hospital and Personal Use Devices
  • Manufacturer
    Medtronic Inc
  • 1 Event
    • Recall of Medtronic Synchromed II Implantable Infusion Pump
SynchroMed® II pump
  • Model / Serial
    Model: , Affected: Model 8637-40 & 8637-20
  • Product Classification
    General Hospital and Personal Use Devices
  • Manufacturer
    Medtronic Inc
  • 1 Event
    • Recall of SynchroMed® II pump
synchromed electronic implantable pumps
  • Model / Serial
  • Product Classification
    General Hospital and Personal Use Devices
  • Product Description
    aimd
  • Manufacturer
    MEDTRONIC
  • 2 Events
    • Field Safety Notices about synchromed electronic implantable pumps
    • Field Safety Notices about synchromed electronic implantable pumps
synchromed electronic implantable pumps
  • Model / Serial
  • Product Description
    aimd
  • Manufacturer
    MEDTRONIC
  • 1 Event
    • Field Safety Notices about synchromed electronic implantable pumps
model 8870 software card used with the n'vision medical programmer model 8840devices for wire...
  • Model / Serial
  • Product Description
    aimd
  • Manufacturer
    MEDTRONIC
  • 1 Event
    • Field Safety Notices about model 8870 software card used with the n'vision medical programmer model 8840devices for wireless control of synchromed drug infusion systems, devices for deep brain neurostimulation (dbs), marrow neurostimulation (scs) and laneurostimulation peripheral (pns).
Synchromed II implantable infusion system (see Annex on 1 sheet)
  • Model / Serial
  • Manufacturer
    Medtronic Inc.
  • 1 Event
    • Recall of Synchromed II implantable infusion system (see Annex on 1 sheet)
Synchromed II
  • Model / Serial
  • Product Classification
    General Hospital and Personal Use Devices
  • Product Description
    medical_device
  • Manufacturer
    MEDTRONIC
  • 3 Events
    • Recall of Synchromed II
    • Recall of Synchromed II
    • Recall of Synchromed II
Device Recall Synchromed II
  • Model / Serial
    Serial numbers: NGP002428N, NGP002429N, NGP002430N, NGP002436N, NGP002437N, NGP002447N, NGP002448N, NGP002495N, NGV001296N, NGV001335N, NGV001390N, NGV001391N, NGV001433N, NGV001447N
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Within the United States and outside the United States.
  • Product Description
    Synchromed II infusion pump
  • Manufacturer
    Medtronic Inc, Neurological & Spinal Division
  • 1 Event
    • Recall of Device Recall Synchromed II
SynchroMed lmplantable Infusion Pump
  • Model / Serial
  • Product Classification
    General Hospital and Personal Use Devices
  • Manufacturer
    Medtronic
  • 2 Events
    • Field Safety Notices about SynchroMed lmplantable Infusion Pump
    • Field Safety Notices about SynchroMed lmplantable Infusion Pump
Synchromed II
  • Model / Serial
  • Product Classification
    General Hospital and Personal Use Devices
  • Manufacturer
    Medtronic
  • 1 Event
    • Field Safety Notices about Synchromed II
SynchroMed II Programmable Implantable Infusion Pump
  • Model / Serial
  • Product Classification
    General Hospital and Personal Use Devices
  • Manufacturer
    Medtronic Inc
  • 1 Event
    • Field Safety Notices about SynchroMed II Programmable Implantable Infusion Pump
SynchroMed II Programmable Implantable Infusion Pump
  • Model / Serial
    Model:8637
  • Product Classification
    General Hospital and Personal Use Devices
  • Manufacturer
    Medtronic Inc.
  • 2 Events
    • Field Safety Notices about SynchroMed II Programmable Implantable Infusion Pump
    • Field Safety Notices about SynchroMed II Programmable Implantable Infusion Pump
SynchroMed II Programmable Implantable Infusion Pump
  • Model / Serial
    Model: 8637
  • Product Classification
    General Hospital and Personal Use Devices
  • Manufacturer
    Medtronic Inc.
  • 1 Event
    • Field Safety Notices about SynchroMed II Programmable Implantable Infusion Pump
Lots CS3643 and CS3663 of the Model 8551 Filling Kit used with Synchromed implantable infusion pumps
  • Model / Serial
  • Manufacturer
    Medtronic Inc
  • 1 Event
    • Recall Or Safety Alert for Lots CS3643 and CS3663 of the Model 8551 Filling Kit used with Synchromed implantable infusion pumps
Software Model 8870 card used in the N'VisionTM 8840 Medical Programmer for SynchroMed® II Im...
  • Model / Serial
  • Manufacturer
    Medtronic Inc
  • 1 Event
    • Recall Or Safety Alert for Software Model 8870 card used in the N'VisionTM 8840 Medical Programmer for SynchroMed® II Implantable Infusion Systems, Models 8637-20, 8637-40 and 8870
N'Vision medical programmer for the Synchromed II pump
  • Model / Serial
  • Manufacturer
    Medtronic Inc.
  • 1 Event
    • Recall Or Safety Alert for N'Vision medical programmer for the Synchromed II pump
Synchromed II® implantable pumps and Synchromed EL
  • Model / Serial
  • Manufacturer
    Medtronic Inc.
  • 1 Event
    • Recall Or Safety Alert for Synchromed II® implantable pumps and Synchromed EL
SynchroMed II implantable infusion pumps
  • Model / Serial
  • Manufacturer
    Medtronic Inc.
  • 1 Event
    • Recall Or Safety Alert for SynchroMed II implantable infusion pumps
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Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.