Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SynchroMed II Infusion Pump. Product Number: 8637-20 Recalled by Medtronic Neuromodulation Due to Potential for error and inability to interrogate pump...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Neuromodulation directly.
Affected Products
SynchroMed II Infusion Pump. Product Number: 8637-20
Quantity: 1 unit
Why Was This Recalled?
Potential for error and inability to interrogate pump due to data corruption in the pump memory.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Neuromodulation
Medtronic Neuromodulation has 95 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report