Medtronic Neuromodulation 2024-10-30 Health serious FDA
Health · FDA · Recall #FDA-Z-0137-2025
SynchroMed II Infusion Pump. Product Number: 8637-20 Recall
Issued October 30, 2024 · Medtronic Neuromodulation
In October 2024, Medtronic Neuromodulation recalled the SynchroMed II Infusion Pump. Product Number: 8637-20, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential for error and inability to interrogate pump due to data corruption in the pump memory.
What you should do
- 1 Stop using SynchroMed II Infusion Pump. Product Number: 8637-20 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medtronic Neuromodulation to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Medtronic Neuromodulation
- Category
- Health
- Recall date
- October 30, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the state of Mississippi.
- Recall number
- FDA-Z-0137-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Medtronic Neuromodulation has 5 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.