San Diego, CA (PRWEB) May 26, 2014 -- AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for Labetalol Hydrochloride Injection.
The FDA announced on May 16, that one lot of Labetalol Hydrochloride Injection 100Mg/20 ML (5MG/ML), 20 ML, Multidose Vial by Hospira is recalled due to embedded particulate within the glass vial identified as stainless steel and visible particles floating in the solution identified as as iron oxide.
Administration of this drug may cause injection site reactions and local irritation in the blood vessels, tissues and organs. In addition, exposure of the particulate to strong magnetic fields could cause tissue damage, according to the FDA.
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 Labetalol Hydrochloride Injection and inform the public. For that reason," he continues, "our focus should squarely fall on investigating these safety alerts and getting the word out.”
As the FDA advises “Anyone with an existing inventory should immediately stop use and quarantine any affected product. In addition, customers should inform potential users of this product in their organizations of this notification.” And the Agency adds “For medical inquiries, please contact Hospira Medical Communications.”
AttorneyOne.com has further information on Labetalol Hydrochloride Injection at the website including latest major drug and medical products law news.
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Sean Burke, Attorney One, http://www.attorneyone.com, +1 (877) 230-7343, [email protected]