Anyone with an existing inventory of the recalled lot should stop use and distribution and quarantine the product immediately
San Diego, CA (PRWEB) October 14, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Vancomycin Hydrochloride.
The FDA announced on October 8, that one lot of Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g Vancomycin (Sterile Powder), by Hospira Inc., is recalled due to uncontrolled storage during transit. FDA’s reason for the recall is that the product may have experienced temperature excursions during shipment to a customer and then was further distributed by the customer.
The affected product is Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g Vancomycin (Sterile Powder), NDC 0409-6533-01, Lot 35-315-DD with expiration date of 01 NOV 2015.
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 Vancomycin Hydrochloride 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 recommends “Anyone with an existing inventory of the recalled lot should stop use and distribution and quarantine the product immediately. Please notify all users in your facility.” And the Agency adds “If you have further distributed the recalled product please notify any accounts or additional locations which may have received the recalled product from you and instruct them if they have redistributed the product to notify their accounts, locations or facilities to the medical facility/retail level.”
AttorneyOne.com has further information on Vancomycin Hydrochloride at the website including the latest major drug, food, and medical products law news.
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