Recall: Hudson RCl Sheridan Endotracheal Tubes
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.
Company Contact Information:
Name: Teleflex Inorated
Do you work for a company involved with this recall? Contact us to learn how you can control data, information and ads shown on this page.
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
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
Latest Safety Recalls
Select image for details, including additional styles.
Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.