Hudson RCI Pediatric Anesthesia Breathing Circuits by Teleflex Medical Recalled (Class I): AttorneyOne Monitors and Keeps Consumers Informed

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On October 7, the FDA announced that Hudson RCI Pediatric Anesthesia Breathing Circuits, by Teleflex Medical, are recalled because the circuit ends may crack or break. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers.

Hudson RCI Pediatric Anesthesia Breathing Circuits Recalled

Hudson RCI Pediatric Anesthesia Breathing Circuits Recalled

use of the products included in the recall may cause serious injuries or death

AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Pediatric Anesthesia Breathing Circuits.

The FDA announced on October 7, that Hudson RCI Pediatric Anesthesia Breathing Circuits, by Teleflex Medical, are recalled because the circuit ends may crack or break. Anesthesia circuits are used in hospitals to care for pediatric patients and deliver a mixture of anesthesia and/or other gases from a mechanical ventilator to a patient.
FDA’s reason for the recall is that the ends of the devices may crack or break before or during use. This could cause serious, life-threatening, health risks, including delayed patient treatment and breathing difficulties if not replaced immediately.

The affected devices’ manufacture dates were from March 2013 to July 2014 and their distribution dates from June 2013 to May 2014.
The FDA classified this recall as Class I, meaning use of the products included in the recall may cause serious injuries or death.

Taking into consideration the latest developments, AttorneyOne.com monitor daily and update the website providing accurate information on all relevant FDA safety alerts. Sean Burke, director of Media Relations at AttorneyOne.com, adds “we are determined to keep an eye on FDA announcements concerning Pediatric Anesthesia Breathing Circuits and inform the public. For that reason", he continues, "our focus should squarely fall on investigating these safety alerts and getting the word out.”

According to the announcement “Teleflex Medical recommends the following actions:
Stop using the devices. Remove the devices from inventory and stop distribution. Return the Recall Acknowledgement Form included with the letter. Notify any customers who may have received the devices through re-distribution.”

AttorneyOne.com has further information on Pediatric Anesthesia Breathing Circuits at the website including the latest major drug, food, and medical products law news.

Headquartered in San Diego, CA Attorney One was founded in 2004 and is not a law firm. They offer a nationwide legal service which helps consumers find the best representation for their legal needs. You can learn more about Attorney One at our website http://www.attorneyone.com. You can also find us on Facebook at http://www.facebook.com/AttorneyOne. Checkout earlier news from us at http://www.prweb.com/releases/2014/09/prweb12235068.htm

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