Medicis Announces Voluntary Recall of Solodyn® (minocycline HCL, USP) 90 Mg Tablets, Extended Release
Medicis Announces Voluntary Recall of Solodyn® (minocycline HCL, USP) 90 Mg Tablets, Extended Release; Lot Numbers B080037 and B080038 Due to Product Mix-UpMedicis today
(May 16, 2008) announced that the Company is voluntarily recalling lot numbers B080037 (Exp: 12/09) and B080038 (Exp: 12/09) of the antibiotic SOLODYN® (minocycline HCl, USP) Extended Release Tablets, 90 mg, 30-count bottles (NDC 99207-461-30)....
FDA Obtains Permanent Injunction Against Scientific Laboratories, Inc.
The U.S. Food and Drug Administration (FDA) today announced that Scientific Laboratories Inc., and its president, Rajeshwari Patel, and chief executive officer, Amit Roy, have signed a Consent Decree of Permanent Injunction and are barred from manufacturing and distributing drug products until they bring their manufacturing operations into compliance with law and obtain approval for their products....
FDA Shuts Down Seafood Processing Company, Requires Products Be Recalled
The U.S. Food and Drug Administration today directed Hope Food Supply Inc., a Pasadena, Texas, food processing company, to shut down and immediately recall all products manufactured from its Texas facility since 2007...
Window Falls Prompts CPSC to Issue Warning
With the arrival of the warmer spring weather, families across the nation are opening their windows to let the fresh air in. This pleasant feeling can quickly turn tragic in households with small children. In recent weeks, several children..
Shindaiwa Corp. Recalls Backpack Blowers Due to Laceration and Impact Hazards
The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed...
Fuel Cells Used With Framing Nailers Recalled by Paslode for Fire Hazard
Name of Product: "Tall Red" Fuel Cells
Units: About 86,000...
Manhattan Group Recalls Infant Rattles Due to Choking Hazard
Name of Product: Tumble Tower Infant Rattles
Units: About 7,000...
Maple Chase Co. Recalls Carbon Monoxide and Carbon Monoxide/Smoke Combo Alarms Due to Alarm Malfunction
Name of Product: FireX Branded 10000 Series Carbon Monoxide (CO) Alarms and 12000 Series CO/Smoke Combo Alarms
Units: About 280,000...
Maran Inc. Children's Hooded Jackets with Drawstrings Recalled Due to Strangulation Hazard; Sold Exclusively at TJ Maxx
Name of Product: Squeeze Kids Girl's Corduroy Jackets
Units: About 6,000...
Atrium Initiates Voluntary Recall Action Regarding HYDRAGLIDE™ Brand Heparin-Coated Thoracic Drainage Catheters used for Autotransfusion during Cardio
Atrium Medical Corporation today (May 15, 2008) announced that it is initiating a voluntary and precautionary recall of selected lots of HYDRAGLIDE™ Brand Heparin-Coated Thoracic Drainage Catheters. Limited lots of Atrium heparin-coated Hydraglide Thoracic Catheters were manufactured with heparin...
Monday, May 19, 2008
Recent Recalls
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