Drugs & medicalClass II

Medtronic Neuromodulation recalls Medtronic SynchroMed II, Model 8637-20, Programmable pump

Medtronic recently identified that if the SynchroMed II pump switches into telemetry mode due to electromagnetic interference (EMI) from an MRI scan, while the pump is sounding an alarm, the pump will not resume drug…

Read the official notice →
Date
2024-01-03
Country
United States
Brand
Medtronic Neuromodulation
Product
Medtronic SynchroMed II, Model 8637-20, Programmable pump
Classification
Class II
Units
Worldwide
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

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