Intravia Containers by Baxter Recalled: AttorneyOne Monitors and Keeps Consumers Informed

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On October 25, the FDA announced that two lots of INTRAVIA containers, by Baxter International, in the U.S. and Canada are recalled due to particulate matter. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers.

Intravia Containers by Baxter Recalled

Intravia Containers by Baxter Recalled

Customers are being directed not to use product from the recalled lots

AttorneyOne.com, a recognized authority on law, updates the website daily regarding all the latest information from the FDA on INTRAVIA containers.

The FDA announced on October 25, that two lots of INTRAVIA containers, by Baxter International, in the U.S. and Canada are recalled due to particulate matter. INTRAVIA containers are empty plastic containers with PVC ports and a sterile fluid path.
The reason for the recall is based on complaints received for particulate matter found inside the fluid path. If the solution containing sterile particulate matter is administered intravenously it may cause adverse health consequences; their extent and severity depend on various factors including the size, number, and composition of the foreign material, and patient’s underlying medical condition.

The affected lots are:

  • INTRAVIA Container, 150 mL Capacity, Lot Number UR13D15112, Product Code 2B8011, distributed to customers between April 26, 2013 and June 20, 2013, and
  • INTRAVIA Container, Empty 500 mL Capacity, Lot Number UR13K14095, Product Code 2B8013, distributed to customers between November 27, 2013 and March 10, 2014.

Taking into consideration the latest developments, AttorneyOne.com monitors daily and updates 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 INTRAVIA containers 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 “Customers are being directed not to use product from the recalled lots.” And the announcement continues “Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.”

AttorneyOne.com has further information on INTRAVIA containers 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/prweb12278013.htm

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Sean Burke
Attorney One
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