ConMed Stat2 Flow Controller Recalled Due to Wrong Component

ConMed_Stat2_Flow_Controller_RecalledThe U.S. Food and Drug Administration (FDA) just announced that a recall has been issued for ICU Medical, Inc.’s ConMed Stat2 Flow Controller.

ICU Medical Inc. is recalling the Stat2 Flow Controller because the device was assembled with a wrong internal component. Because of this, the Flow Controller may deliver fluid at a much higher flow rate than for what it was set.

The recall has been deemed a Class I by the FDA, which means that use of the affected product may cause serious adverse health consequences, including death.

The recall date is August 19, 2014 and involves the ConMed Stat2 Flow Controller, which is used in intravenous (IV) administration sets.

The recalled devices were manufactured from October 2013 through January 2014 and were also distributed from October 2013 through January, 2014.

The item numbers involved are 011-C9801, 011-C9802, AH7007, B9897, Z2648 and the impacted lot numbers are 2768416, 2768417, 2758229, 2785379, 2801951, 34-128-HE, 34-540-Y1, 35-151-SJ, 35-805-JW, 36-137-SL, 36-469-SL

The recalled medical device is used with IV administration sets that contain hypodermic needles and tubing. The devices are used to deliver or remove fluids from the body, in humans or animals. The amount of fluid delivered is controlled by a flow controller.

On August 19, 2014, ICU Medical Inc. issued an Urgent Medical Device Recall Notification letter to affected customers and authorized distributors. The letter identified the affected, recalled product; the problem with the device; and the actions to be taken. The letter advises customers to:

  • Remove the affected ICU Medical, Inc.’s ConMed Stat2 Flow Controller devices from use and to return the recalled device to ICU Medical, Inc.
  • Complete sections A and B of the Recall Response Form included with the letter and to return the completed form to ICU Medical.
  • Contact ICU Customer Care at (866) 829-9025 and select option 8 for a Return Goods Authorization. Customers may also E-mail:

Customers will be credited for any returned product.

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