FDA recall notice for KIT,DISPOSABLE ACCESSORY,4ARM,IS2000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment fr
FDA recall notice for AUTOMIX High Speed Compounder System, product 2M8077; automated nutrition compounders; Product Usage: The Automix Compounder Systems
FDA recall notice for KIT,DISPOSABLE ACCESSORY,3ARM,IS3000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment fr
FDA recall notice for Strawberry Filled Cake, 21.9 oz (1lb 6oz) (620g), UPC 3 760147 195867 (Authentic Gourmet). Reason: The recall was initiated because Authen
FDA recall notice for Raspberry Filled Cake, 21.9 oz (1lb 6oz) (620g), UPC 3 760147 195881 (Authentic Gourmet). Reason: The recall was initiated because Authent
FDA recall notice for Nature's Grain Garlic French Bread, 10 oz (284 g) packages, (Southern Bakeries, LLC). Reason: Southern Bakeries, Hope, AR is recalling its
CPSC recall notice for Old Navy Toddler Girl Aqua Socks. Reason: The slip-on shoes have pull-on tabs on both the front and back of the foot open…. Issued 2012-0
CPSC recall notice for Chicco Polly High Chair. Reason: This recall involves a range of Chicco Polly high chairs with pegs on the back…. Issued 2012-07-12.
FDA recall notice for Wildwood Organic Medium Salsa , 14 oz, Pack size 6/14 oz per case. Packaged in plastic cup, sealed with film and capped with plastic cap.
FDA recall notice for Wildwood Organic Mild Salsa , 14 oz, Pack size 6/14 oz per case. Packaged in plastic cup, sealed with film and capped with plastic cap. Pr
FDA recall notice for Wildwood Emerald Valley Kitchen Organic Mild Salsa - Canada (containing French in labeling), 397 mL. Pack size 6/14 oz per case. Packaged
FDA recall notice for Wildwood Emerald Valley Kitchen Organic Medium Salsa, 30 oz. Pack size 6/30 oz per case, 14 oz Pack size 6/14oz per case, Packaged in
FDA recall notice for ACUSON SC2000 ultrasound systems at software versions VA20A or VA20B. Model number 10433816. The SC2000 ultrasound imaging system is i
FDA recall notice for Adult Resuscitator, Pro-5000 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressure monitor is inte
FDA recall notice for Safe Spot Infant Resuscitator, Pro-1900 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressure moni