Friday, June 29, 2012

Bedford Laboratories Issues Voluntary Hospital/User-Level Recall Of Vecuronium Bromide For Injection Preservative Free, Lot 2067134, Because Of Health Risk

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

06/29/2012 10:35 AM EDT

Bedford Laboratories today announced a nationwide voluntary hospital/user‐level recall for: Vecuronium Bromide for Injection, 20 mg vial – NDC #55390‐039‐10 Lot 2067134 – Exp. Date 5/31/2013 First Shipment – 8/8/2011 Last Shipment – 11/9/2011 Please note: This recall is for lot 2067134 only. No other lots of Vecuronium Bromide for injection Preservative Free are subject to this voluntary recall.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.


This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420 Powered by GovDelivery

No comments:

Post a Comment