Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc. Due to A small number of specific pumps may trigger...
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 Codman & Shurtleff, Inc. directly.
Affected Products
MedStream Programmable Infusion Pump, 20 mL, Product Code: 91-4200 The MedStream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market.
Quantity: 90
Why Was This Recalled?
A small number of specific pumps may trigger a low battery alarm at the beginning of the implanted life.
Where Was This Sold?
Worldwide Distribution including the countries of Belgium Germany, Spain, United Kingdom, Ireland, Italy, Russia and Turkey.
About Codman & Shurtleff, Inc.
Codman & Shurtleff, Inc. has 58 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report