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Home > Recalled Products > Medical Devices > Defect > Hudson RCl Sheridan Endotracheal Tubes

Recall: Hudson RCl Sheridan Endotracheal Tubes

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On 2019-06-25, the FDA announced that Teleflex Inorated is conducting a recall on Endotracheal Tubes due to a possible . The recalled products were sold under the brand name(s) Hudson RCl Sheridan during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 4 medical devices recalls due to potential defect, including infant warmers ge healthcare's giraffe and panda i-res infant warmers, hamilton g5 ventilators and more. Additionally, there have been 1 drug and medical device recalls due to other health hazards as well as 67 food recalls.

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Teleflex Incorporated, Logo
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Company Contact Information:

Name: Teleflex Inorated
Website: www.teleflex.com
Phone: 1-866-396-2111

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Detailed Recall Information



Regions Where Sold: Nationwide

Product Description: Endotracheal Tubes

Brand Name(s): Hudson RCl Sheridan

Reason for Recall: Defect

Official Recall Date: 2019-06-25


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Additional information provided by the FDA.gov:

Teleflex Incorporated (NYSE: TFX), has announced a worldwide recall of certain lots of Hudson RCI@ Sheridan@ Endotracheal Tubes. The recalled products are designed for oral or nasal intubation and are indicated for airway management. The products involved in this recall are as follows: Read More.


More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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