Medtronic Neuromodulation: Medical Device Recalls in 2019

According to to data from the FDA, there were 2 medical device recalls made by Medtronic Neuromodulation in 2019. See the details of the recalls below.

You can see similar recalls for other firms.

• Synchromed II programmable pump, Model numbers 8637-20 and 8637-40
• InterStim(TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usage: The Medtronic Model A510 Clinician application (app) is intended for use with the HH90 Handset and TM90 Communicator to program, adjust, and troubleshoot the Medtronic Models 3023 and 3058 InterStim neurostimulators for sacral neuromodulation therapy. The clinician uses the Clinician app to program settings for the patient. The A510 Clinician app, HH90 Handset, TM90 Communicator along with the A520 Patient app are only sold as a kit (TH90).