Codman & Shurtleff, Inc.: Medical Device Recall in 2013 - (Recall #: Z-2293-2013)

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 Pump; 20ml - 91-4200US Product Usage: 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. Refill Kits- are intended for use in the filling and re-filling of the Medstream pump reservoir.

Product Classification:

Class I

Date Initiated: August 13, 2013

Date Posted: October 9, 2013

Recall Number: Z-2293-2013

Event ID: 65821

Reason for Recall:

Drug flow rates exceeding programmed flow rates.

Status: Terminated

Product Quantity: 2 units

Code Information:

Lot/Serial Number US: NMBJ7K, NMBJ5C

Distribution Pattern:

Worldwide Distribution - USA Nationwide in the states of NJ, NC, TX, FL and in the countries of Austria, Belgium, Egypt, Germany, Greece, Ireland, Israel, Italy, Luxemborg, Portugal, Russia, Saudi Arabia, Slovenia, Spain, Sweden, Switzerland, Turkey, and UK.

Voluntary or Mandated:

Voluntary: Firm initiated