Recall Class: Class I Date Recall Initiated: September 22, 2009 Product: Premie Pack, Kit Code LM 110 and Full Term Meconium Pack, Kit Code LM115 Model Lot/Serial Numbers  NOTE: These are the Portex uncuffed pediatric sized tracheal tubes which were subject to the Class I recall with Smiths Medical. 2.5 mm product code … [Read more...]

Shirley, NY - American Regent conducts nationwide voluntary recall of ALL lots of its Ketorolac Tromethamine Injection, USP 15 mg/mL: NDC# 0517-0601-25 15 mg/mL 1mL Single Dose Vial PLEASE NOTE: This recall is in addition to the voluntary recall initiated on October 16, 2009 when American Regent voluntarily recalled ALL unexpired lots of … [Read more...]

This post has been moved to: Bodybuilding.com Supplements May Contain Steroids. … [Read more...]

Pointe Scientific, Inc. is recalling all size kits of Liquid Glucose Hexokinase Reagent catalog number G7517. The reagents have been found to fail linearity at >200mg/dL that results in inaccurate glucose values above this range. Distributors and testing laboratories who have received the Pointe Scientific, Inc Liquid Glucose Hexokinase Reagent … [Read more...]

Cordis Corporation announced today a nationwide voluntary recall of all lots of the CROSSOVER™ Sheath Introducer due to complaints about stretching or fracture of the sheath during use. The CROSSOVER Sheath Introducer is a product developed and manufactured by Thomas Medical Products, Inc., and distributed by Cordis. It is a long-coil reinforced, … [Read more...]