NOVABUS ( 09V494000 )
Dated: DEC 15, 2009 NOVA BUS IS RECALLING MODEL YEAR 2009 LFS BUSES EQUIPPED WITH Q’STRAINT MAX MOBILITY DEVICE REMOTE RELEASE BELTS USED ON AMERICAN INSIGHT TRANSVERSE FLIP UP SEATS WITH BUILD DATES BETWEEN OCTOBER 2008…
Dorel Juvenile Group Recalls Play Yards with Bassinets Due to Suffocation Hazard
The one piece metal bars supporting the floorboard of the bassinet attachment can come out of the fabric sleeves and create an uneven sleeping surface, posing a risk of suffocation or positional asphyxiation.
Dehumidifiers Recalled by LG Electronics Tianjin Appliance Due to Fire and Burn Hazards
The power connector for the dehumidifier’s compressor can short circuit, posing fire and burn hazards to consumers.
Wooden Toys Recalled by Kendamaspot Due to Violation of Lead Paint Ban
The surface paint coating on the ball contains excessive levels of lead, violating the federal lead paint standard.
GILLIG ( 09V493000 )
Dated: DEC 16, 2009 GILLIG IS RECALLING MODEL YEAR 2008-2009 LOWFLOOR BUSES EQUIPPED WITH Q’STRAINT MAX MOBILITY DEVICE REMOTE RELEASE BELTS USED ON AMERICAN INSIGHT TRANSVERSE FLIP UP SEATS WITH BUILD DATES BETWEEN OCTO…
Janzen Farms Recalls Hazelnut Kernels Because of Possible Health Risks
Janzen Farms, Dayton, Oregon is recalling hazelnut kernels because the product has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
Tylenol Arthritis Pain Caplet, 100 count bottles: Recall of all lots
Recall expanded from November recall of 5 lots due to reports of moldy, musty, or mildew-like odor that was associated with nausea, stomach pain, vomiting and diarrhea. Posted 12/28/2009
Thermoflect Blankets and product line - Recall
FDA recommends blankets and other products not be used in magnetic resonance [MR] conditional or MR compatible environments
Mcneil Consumer Healthcare Announces A Voluntary Nationwide Recall Of All Lots Of Tylenol® Arthritis Pain 100 Count With Ez-Open Cap
In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is expanding its voluntary recall to include all available product lots of TYLENOL® Arthritis Pain Caplet 100 count bottles, with the distinctive red EZ-OPEN CAP (Full list of lot numbers provided below).
Encompass Group Voluntarily Recalls Thermoflect Product Line
Jea R. Gackowski, Encompass Group Corporate Compliance Officer announced today the company is voluntarily recalling the Thermoflect product line for relabeling regarding its use in the MR (Magnetic Resonance) environment.