Recalls for Cook Medical

Beacon Tip Angiographic Catheters by Cook Medical: Class 1 Recall - Catheter Tip May Slip or Separate
08/07/2015 Medical Recall

If this occurs, the tip could enter the patient’s bloodstream. This could cause serious injury to the patient and require additional medical intervention to retrieve the tip, or cause death.

  • Company:
    Cook Medical
Cook Medical Issues Global Recall Of Beacon Tip Angiographic Catheter Products
08/04/2015 Food Recall

On July 2, 2015, Cook Medical initiated a lot-specific voluntary recall of 2,239 lots of Beacon Tip Angiographic Catheters. Globally, 95,167 devices are subject to this recall. The products include specific versions and lot numbers of the Torcon NB® Advantage Beacon® Tip Catheters (Catalog Prefix HNBR5.0), Royal Flush® Plus Beacon® Tip High-Flow Catheters (Catalog Prefix HNR4.0), and Slip-Cath® Beacon® Tip Catheters (Catalog Prefix SCBR5.0).

  • Company:
    Cook Medical
  • Problem
    The Beacon Tip Angiographic Catheters have been found to exhibit tip splitting or separation.
UPDATED: CloverSnare™ 4-Loop Vascular Retrieval Snare Recall
08/27/2014 Food Recall

On July 10, 2014, Cook Medical initiated a recall of 696 of its CloverSnareâ„¢ 4-Loop Vascular Retrieval Snare devices. The device was recalled because of a potential for the loop to separate from the shaft, resulting in loss of device function, potential for embolization of snare fragments and the potential need for intervention to retrieve the separated snare.

  • Company:
    Cook Medical
  • Problem
    May Contain Undeclared Pine Nuts (Tree Nuts).
CloverSnare 4-Loop Vascular Retrieval Snare by Cook Medical: Recall - Risk of Loop to Separate From Shaft
08/20/2014 Medical Recall

Use of affected product may result in loss of device function, potential for embolization of snare fragments, and the potential need for intervention to retrieve the separated snare.

  • Company:
    Cook Medical
CloverSnare™ 4-Loop Vascular Retrieval Snare Recall
08/20/2014 Food Recall

On July 10, 2014, Cook Medical initiated a recall of 696 of its CloverSnare™ 4-Loop Vascular Retrieval Snare devices. The device was recalled because of a potential for the loop to separate from the shaft, resulting in loss of device function, potential for embolization of snare fragments and the potential need for intervention to retrieve the separated snare.

  • Company:
    Cook Medical
  • Problem
    May Contain Undeclared Pine Nuts (Tree Nuts).