http://www.usfa.fema.gov/rss/alerts.xml Advisories to keep fire service personnel up to date on equipment recalls and safety alerts. Wed, 12 Jun 2013 14:51:00 EDT en-us Sagent Pharmaceuticals, Inc. has announced the voluntary nationwide recall of three lots of Vecuronium Bromide for Injection 10mg (NDC number 25021-657-10) manufactured by Mustafa Nevzat Ilac Sanayii A.S. (MN Pharmaceuticals) and distributed by Sagent. Sagent has initiated this voluntary recall of Vecuronium Bromide for Injection to the user level due to the discovery of an elevated impurity result detected during routine quality testing of stability samples at the 18-month interval. http://www.fda.gov/Safety/Recalls/ucm356010.htm Wed, 12 Jun 2013 14:51:00 EDT http://www.fda.gov/Safety/Recalls/ucm356010.htm The signaling device can malfunction when used and restrict the diver's air flow, posing a drowning hazard. http://www.cpsc.gov/en/Recalls/2013/DiveAlert-Emergency-Signaling-Devices-Recalled-by-Ideations/ Wed, 12 Jun 2013 14:51:00 EDT http://www.cpsc.gov/en/Recalls/2013/DiveAlert-Emergency-Signaling-Devices-Recalled-by-Ideations/ Fresenius Kabi USA announced it has initiated a voluntary recall of one lot - Lot 6103882 - of Magnesium Sulfate Injection, USP due to the potential presence of glass particles in the vials. The recall is a precautionary measure, following a routine company inspection of retained product samples. http://www.fda.gov/Safety/Recalls/ucm354238.htm Mon, 02 Jun 2013 20:25:00 EDT http://www.fda.gov/Safety/Recalls/ucm354238.htm