Codman & Shurtleff, Inc.: Medical Device Recall in 2013 - (Recall #: Z-1690-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery of Baclofen or Morphine Product Code:91-4200 (20ml pump) US 91-4200. Intended for the intrathecal delivery of Baclofen or Morphine.

Product Classification:

Class I

Date Initiated: June 7, 2013

Date Posted: July 24, 2013

Recall Number: Z-1690-2013

Event ID: 65420

Reason for Recall:

Miscalibrated Fill Level Sensor may affect dosing level

Status: Terminated

Product Quantity: 2 units US and 735 OUS

Code Information:

All serial numbers

Distribution Pattern:

Worldwide Distribution-USA (nationwide) including the states of FL, NC, NJ, and TX, and the countries of Austria, Belgium, Spain, Great Britain, Germany, Italy, Ireland, Luxemburg, Russia, Saudi Arabia, Portugal, Greece, Egypt, Switzerland, and Turkey.

Voluntary or Mandated:

Voluntary: Firm initiated