Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc. Due to Miscalibrated Fill Level Sensor may affect dosing level
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 , Implantable for the intrathecal delivery of Baclofen or Morphine Product Code: 91-4201US (40ml pump) 91-4201 (40ml pump) Intended for the intrathecal delivery of Baclofen or Morphine.
Quantity: 5 US and and 360 OUS
Why Was This Recalled?
Miscalibrated Fill Level Sensor may affect dosing level
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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