Reported Jul 24, 2013 · Terminated

MedStream Programmable Infusion Pump , Implantable for the intrathecal delivery of Baclofen or Morphine Product Code:…

Codman & Shurtleff, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Codman & Shurtleff, Inc. · 325 Paramount Drive · Raynham, MA · 02767

Is this the product you have?

  • MedStream Programmable Infusion Pump , Implantable for the intrathecal delivery
  • of Baclofen or Morphine Product Code91-4201US (40ml pump) 91-4201 (40ml pump) Intended for the intrathecal delivery of Baclofen or Morphine
Lot codes and dates
  • All serial numbers
Amount recalled
5 US and and 360 OUS

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was recalled

Stop using this product now

Miscalibrated Fill Level Sensor may affect dosing level

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 21, 2015 · Data as of Sep 19, 6:48 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.