Reported Oct 30, 2024 · Ongoing
SynchroMed II Infusion Pump. Product Number: 8637-20
Medtronic Neuromodulation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Neuromodulation · 7000 Central Ave Ne · Minneapolis, MN · 55432-3568
Is this the product you have?
- SynchroMed II Infusion Pump
- Product Number8637-20
- Lot codes and dates
- GTIN Number00643169630505
- Serial NumberNGP004814H
- Amount recalled
- 1 unit
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
- MS
Why it was recalled
Potential for error and inability to interrogate pump due to data corruption in the pump memory.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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