|
Celeste Industries Corporation Recalls All Lots of simplySmart Remove Make Up Remover (January 5) Celeste Industries Corporation has voluntarily recalled all lots of simplySmart Remove Make Up Remover in the US and Canada This product is packaged as a single towelette with hiexpress.com shown on the packet. This recall was a result of certain...Viking Range Corp. Recalls Toasters Due to Shock Hazard Wiring inside the toaster can become loose and contact the toaster body, posing a shock hazard to consumers.Bicycles with RockShox Bicycle Forks Recalled by SRAM LLC Due to Crash Hazard The steel steerer on the forks can crack, causing the fork to detach from the bicycle frame. This can cause the rider to lose control and crash.Children's Hooded Jackets with Drawstrings Recalled by Ms. Bubbles Inc. Due to Strangulation Hazard The jackets have a drawstring through the hood which can pose a strangulation hazard to children. In February 1996, CPSC issued guidelines to help prevent children from strangling or getting entangled on the neck and waist drawstrings in upper garments,...Jardine Expands Recall of Cribs Sold by Babies"R"Us; Cribs Pose Entrapment and Strangulation Hazards The wooden crib slats can break, creating a gap, which can pose an entrapment and strangulation hazard to infants and toddlers.National Brands Inc. Issues a Nationwide Recall of Topaz brand Wafer Rolls Because of Possible Health Risks (December 19) National Brands Inc., Spring Valley NY is initiating a nationwide recall of all their 4.76oz (135gm) cans and 12.3oz (350gm) cans of Topaz brand Wafer Rolls because it may be contaminated with...FDA Announces Class I Recall of Ophthalmic Surgical Device The U.S. Food and Drug Administration announced a Class I recall of lot no. UD30654 of Healon D, an ophthalmic viscosurgical device (OVD) manufactured by Advanced Medical Optics Inc. (AMO) of Santa Ana,...Stryker Craniomaxillofacial Issues Nationwide Recall of its Custom Cranial Implant Kits; Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104, all lots shipped sterile (December 23) Stryker's Craniomaxillofacial (CMF) business unit announced today that the U.S. Food and Drug Administration (FDA) concluded on Dec. 18, 2008 that its recall of the following Stryker CMF's Custom Cranial Implant Kits is a Class I recall, which means the...Boys Reversible Vests Recalled by Bon-Ton Stores Due to Choking Hazard The zipper tabs on these vests fail to meet the children's torques test standards, posing a choking hazard to children.Faulty Instructions Prompt Recall of Electrical Wiring How-to-Books by The Taunton Press; Shock Hazard to Consumers The books contain several errors in the technical diagrams that could lead consumers to incorrectly install or repair electrical wiring, posing an electrical shock hazard to consumers. ###
|
