San Diego, CA (PRWEB) June 16, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Portex Low Dead Space Connector.
The FDA notified on June 13, of a Class I recall of Smiths Medical Portex Low Dead Space Connector with Sideport because one lot of 3.0mm sized connectors were mislabeled in packages as 3.5mm. Portex Low Dead Space Connector is used to attach the endotracheal tube to the patient breathing circuit for respiratory support.
The affected lot number is Lot #2553426 and was distributed in November 2013. 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 Portex Low Dead Space Connector and inform the public. For that reason", he continues, "our focus should squarely fall on investigating these safety alerts and getting the word out.”
The FDA advises “Customers should examine their inventory, remove all affected products and returned the completed Response Form and affected products to Smith Medical.”
AttorneyOne.com has further information on Portex Low Dead Space Connector at the website including latest major drug and medical products law news.
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