Since Actemra (tocilizumab) hit the market in 2010, the U.S. Food and Drug Administration (FDA) has received at least 13,500 adverse event reports link to the drug, including 1,128 reports of death, according to a recent investigation by STAT. Actemra was approved to treat rheumatoid arthritis (RA) in 2010. In May 2017, the FDA approved Actemra for … [Read more...]
TRAIL KING ( 17V494000 )
Dated: AUG 04, 2017 Trail King Industries, Inc. (Trail King) is recalling certain 2012-2014 TK70HDG, TK80HDG, TK102HDG, TK110HDG, and TK110HED gooseneck trailers. The pivot plate reinforcement in the gooseneck pivot are... … [Read more...]
RAM ( 17V499000 )
Dated: AUG 10, 2017 Streetcar ORV LLC, dba American Expedition Vehicles (AEV) is recalling certain 2013-2017 RAM 2500 and 3500 heavy duty trucks, modified by AEV to be equipped with cast aluminum Katla 8.5" road wheels. ... … [Read more...]
INTERNATIONAL ( 17V406000 )
Dated: AUG 14, 2017 Navistar Inc. (Navistar) is recalling certain 2018 International LT and HX severe service diesel trucks equipped with Cummins ISX 15L engines. These engines have a fuel pump whose drive gear could po... … [Read more...]
CROSSROADS ( 17V505000 )
Dated: AUG 14, 2017 Keystone RV Company (Keystone) is recalling certain 2018 Crossroads Redwood and Cameo recreational trailers. The propane manifold under the kitchen slide may contact the floor potentially causing dam... … [Read more...]
RIDE THE DUCKS ( 17V501000 )
Dated: AUG 11, 2017 Ride the Ducks International LLC (RTDI) is recalling certain 1996-2005 "Stretch" Amphibious Passenger Vehicles. Due to excessive fatigue, the front axle housing on the affected vehicles may fracture ... … [Read more...]
FOREST RIVER ( 17V500000 )
Dated: AUG 10, 2017 Forest River, Inc. (Forest River) is recalling certain 2016-2017 Berkshire vehicles built on Freightliner Custom Chassis XCR chassis. A battery cable mounting bracket may not have been installed corr... … [Read more...]
KME ( 17V503000 )
Dated: AUG 14, 2017 Kovatch Mobile Equipment Corp. (KME) is recalling certain 2014-2016 Predator SS Aerial, and Predator Aerial vehicles. The software that controls the ladder rotation circuit may allow the ladder to ro... … [Read more...]
KME ( 17V504000 )
Dated: AUG 14, 2017 Kovatch Mobile Equipment Corp. (KME) is recalling certain 2012-2014 Predator Aerial, and 2014-2017 Predator SS Aerial vehicles. A software error may cause the aerial ladder tip control speed to momen... … [Read more...]
HINO ( 17V493000 )
Dated: AUG 07, 2017 Hino Motor Sales U.S.A., Inc. (Hino) is recalling certain 2018 NE8J, NJ8J, and NV8J vehicles. The door hinge bolts on these vehicles may not be sufficiently tightened, possibly allowing the door to o... … [Read more...]
NEWMAR ( 17V497000 )
Dated: AUG 09, 2017 Newmar Corporation (Newmar) is recalling certain 2014 Moutain Aire and 2014-2017 Dutch Star recreational vehicles built on Freightliner XCR chassis manufactured by Daimler Trucks North America (DTNA).... … [Read more...]
TEMSA ( 17V498000 )
Dated: AUG 10, 2017 Temsa Global Sanayi Ve Ticaret A.S. (Temsa) is recalling certain 2014-2018 TS45 coach buses. The hydraulic steering hose for the tag axle steering system may leak or burst during operation or service... … [Read more...]
Polaris Recalls GENERAL Recreational Off-Highway Vehicles Due to Crash Hazard (Recall Alert)
Inconsistent tire pressure information can result in improperly-inflated tires, posing a crash hazard. … [Read more...]
Bella Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of All Sterile Drug Products Due to Lack of Sterility Assurance
Bella Pharmaceuticals is voluntarily recalling all lots of unexpired sterile drug products due to lack of sterility assurance. The recalled products were distributed to health care facilities nationwide. Administration of a drug product intended to be sterile that is not sterile could result in serious infections that may be … [Read more...]
Vital Rx, Inc. d/b/a Atlantic Pharmacy and Compounding Issues Voluntary Nationwide Recall of all Compounded Injectable Prescription Medications Due to Lack of Sterility Assurance
Vital Rx, Inc. d/b/a Atlantic Pharmacy and Compounding is voluntarily recalling all lots of all compounded injectable prescription medications to the consumer level. The compounded injectable prescription medications have been found to lack sterility assurance. Atlantic Pharmacy and Compounding became aware of this issue during an FDA (Food and … [Read more...]
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