FDA Enforcement Class I Terminated

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.

Recall: Z-1690-2013 · Reported July 24, 2013

Enforcement

Recall Number
Z-1690-2013
Event ID
65420
Classification
Class I
Status
Terminated
Product Type
Devices
Firm
Codman & Shurtleff, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 24, 2013
Initiation Date
June 7, 2013
Classification Date
July 16, 2013
Termination Date
April 21, 2015
Address
325 Paramount Drive, N/A, Raynham, MA, 02767, United States

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.

Reason

Miscalibrated Fill Level Sensor may affect dosing level

Code Info

All serial numbers

Distribution

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.

Quantity

2 units US and 735 OUS