Codman & Shurtleff, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1572-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

MedStream Programmable Infusion Pump, 40 mL, Product Code: 91-4201 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.

Product Classification:

Class II

Date Initiated: November 10, 2015

Date Posted: May 21, 2014

Recall Number: Z-1572-2014

Event ID: 67921

Reason for Recall:

A small number of specific pumps may trigger a low battery alarm at the beginning of the implanted life.

Status: Terminated

Product Quantity: 34

Code Information:

Serial Numbers: NNBLV3, NNBLHF, NNBLK4, NNBLV4, NNBLV6, NPBL9F, NPBL89, NPBL8R, NPBL8T, NPBL9B, NPBL77, NPBL2K, NPBL8V, NPBL9D, NPBL8C, NNBLHH, NNBLHD, NNBLHB, NNBLHJ, NNBLHC, NNBLHG, NNBLV7, NNBLV5, NNBLV0, NNBLWC, NPBL2G, NPBL1F, NPBL1D, NPBL1B, NPBL09, NPBL88, NPBL7R, NPBL2N, NPBL6Z

Distribution Pattern:

Worldwide Distribution including the countries of Belgium Germany, Spain, United Kingdom, Ireland, Italy, Russia and Turkey.

Voluntary or Mandated:

Voluntary: Firm initiated