Kiriko, LLC. is voluntarily recalling all lots of A1 Slim 30 capsules bottle to the consumer level. FDA laboratory analysis has found the A1 Slim product to be tainted with sibutramine, phenolphthalein and N-Desmethyl sibutramine. These undeclared ingredients make this product an unapproved new drug for which safety and efficacy have … [Read more...]
FORD ( 17V594000 )
Dated: SEP 25, 2017 Ford Motor Company (Ford) is recalling certain 2015 F-650 and F-750 trucks, equipped with certain Spicer D-Series and E-Series steer axles. The castellated nut on the steer axles may not be properly ... … [Read more...]
FLEETWOOD ( 17V584000 )
Dated: SEP 20, 2017 REV Recreation Group (REV) is recalling certain 2013-2015 Fleetwood Bounder and 2013-2016 Fleetwood Southwind recreational vehicles. The welds attaching the battery tray may be insufficient. As a re... … [Read more...]
THOMAS BUILT BUSES ( 17V589000 )
Dated: SEP 21, 2017 Daimler Trucks North America LLC (DTNA) is recalling certain 2014-2018 Thomas Built Buses Saf-T-Liner HDX and Saf-T-Liner C2 transit buses. A reinforcement bracket may be missing from the seats that ... … [Read more...]
JAYCO ( 17V590000 )
Dated: SEP 22, 2017 Jayco, Inc. (Jayco) is recalling certain 2016-2017 Greyhawk motorhomes, model 29ME. Damage to the liquid propane (LP) line can occur by the line being melted by the vehicle's exhaust pipe, contacting... … [Read more...]
KEYSTONE ( 17V597000 )
Dated: SEP 25, 2017 Keystone RV Company (Keystone) is recalling certain 2008-2009 Raptor recreational vehicles, models 3110 and 3018, equipped with IOTA ITS-50R transfer switches. These transfer switches may fail when e... … [Read more...]
BMW ( 17V591000 )
Dated: SEP 22, 2017 BMW of North America, LLC (BMW) is recalling certain 2014-2016 F800 GT and 2015-2016 F800 R motorcycles. The rear side reflex reflectors on these vehicles may not be properly visible in certain traff... … [Read more...]
KIA ( 17V586000 )
Dated: SEP 21, 2017 Kia Motors America (Kia) is recalling certain 2017 Sorento vehicles equipped with 3.3L engines. The engine crankshaft may have been improperly heat treated and may fail. … [Read more...]
GLAVAL ( 17V585000 )
Dated: SEP 21, 2017 Forest River, Inc. (Forest River) is recalling certain 2017-2018 Glaval Bus Apollo, Commute, Concorde II, Entourage, Legacy, Primetime, Titan II, Titan II Low Floor, and Universal transit buses. The ... … [Read more...]
HYUNDAI ( 17V577000 )
Dated: SEP 20, 2017 Hyundai Motor America (Hyundai) is recalling certain 2018 Santa Fe Sport vehicles. The front coil springs may have been improperly manufactured and, as a result, may fracture under certain loads whil... … [Read more...]
THOMAS BUILT BUSES ( 17V587000 )
Dated: SEP 21, 2017 Daimler Trucks North America LLC (DTNA) is recalling certain 2014-2018 Thomas Built Buses Saf-T-Liner HDX and Saf-T-Liner C2 school buses. A reinforcement bracket may be missing from the seats that h... … [Read more...]
MITSUBISHI ( 17V569000 )
Dated: SEP 14, 2017 Mitsubishi Motors North America, Inc. (Mitsubishi) is recalling certain 2004-2006 Lancer and Lancer Evolution vehicles and 2004 Lancer Sportback vehicles. These vehicles are equipped with a passenger... … [Read more...]
HYUNDAI ( 17V578000 )
Dated: SEP 20, 2017 Hyundai Motor America (Hyundai) is recalling certain 2017 Santa Fe vehicles equipped with 3.3L engines. The crankshaft assemblies may have been produced with surface irregularities in the crankshaft ... … [Read more...]
Sandridge RMH Acquisition, LLC Recalls Ready-To-Eat Beef Products Due To Misbranding and Undeclared Allergens
WASHINGTON, Oct. 5, 2017 – Sandridge RMH Acquisition, LLC, a Morton Ill. establishment, is recalling approximately 1,222 pounds of ready-to-eat beef products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products are mislabeled as beef pot … [Read more...]
Baxter Initiates Voluntary Nationwide Recall of One Shipment of Intralipid 20% IV Fat Emulsion Due to Product Being Exposed to Subfreezing Temperatures
Baxter International Inc. announced today it is voluntarily recalling one shipment from a single lot of INTRALIPID 20% IV Fat Emulsion, 100 mL, distributed between 8/11/17 and 8/31/17 to hospitals and healthcare providers in the United States, to the user level. The product has been exposed to subfreezing temperatures during transit to a … [Read more...]
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