State
73,833 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.
Which agencies issued them
These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
LS Import is recalling about 660 airplane and butterfly push toys because detachable parts pose a choking hazard to young children.
Mima is recalling Moon 3-in-1 high chairs because the seat can loosen and dislodge, posing a fall and impact hazard to children.
Sea Gull Lighting is recalling about 8,800 chandeliers in the U.S. and 800 in Canada because the screw collar can break, causing the fixture to fall.
Hospira Inc. is recalling 126,075 vials of Propofol Injectable Emulsion because a complaint reported an embedded iron particulate in one vial.
Eillien's Candies, Inc. is recalling specific lots of walnut pieces nationwide due to potential Salmonella contamination.
Newmar is recalling 2015 Essex motorhomes because the steering shaft may disconnect or slip, increasing the risk of a crash.
Utility Trailer Manufacturing Company is recalling 2014-2015 trailers because a brake actuator defect may cause overheating and fire.
General Motors is recalling specific 2006-2007 Chevrolet Malibu, Malibu Maxx, and Pontiac G6 vehicles because the electric power steering assist may suddenly fail, increasing crash risk.
Lifesmart is recalling Lifepro portable mini space heaters because the back plate can detach, posing an electrical shock hazard. No injuries have been reported.
Morgan Olson is recalling 11 model year 2014 Service Body trucks because rear identification and license plate lamps may be mounted incorrectly, reducing visibility.
Family Dollar is recalling Tough Treadz Auto Carrier toy sets because the die-cast metal cars have sharp edges that pose a laceration hazard.
Sunrise Medical is recalling three Zippie Zone Pediatric Rigid Wheelchairs because the height-adjustable handle may dislodge due to failing locking mechanisms.
Lazy One is recalling about 8,400 children's pajamas and robes because they fail to meet federal flammability standards, posing a burn hazard.
Piaggio is recalling specific Vespa and Piaggio motorcycles because a defective fuel pump may cause the vehicle to stall or fail to restart, increasing crash risk.
Philips is recalling 1,064 BrightView MRI systems worldwide due to software issues causing unintended detector and gantry movement.
Clinical Innovations, LLC is recalling 827 units of the Ebb Complete Tamponade System because of a potential for balloon leaks in lots manufactured since August 2014.
Baxter Healthcare is recalling HomeChoice and HomeChoice Pro automated peritoneal dialysis cyclers because the keypad buttons may activate without being pressed.
Sunrise Medical is recalling six Quickie Q7 Adult Rigid Wheelchairs because the height-adjustable handle may dislodge due to failing locking mechanisms.
Beckman Coulter is recalling Lipase Assay kits because N-acetyl cysteine can cause falsely low results.
Aesculap, Inc. is recalling Miethke Shunt System accessories because the shelf box labels incorrectly display an MR conditional symbol. The product is actually MR unsafe, and the correct information is only provided in the Instructions for Use.
Beckman Coulter is recalling Uric Acid Assay kits because N-acetyl cysteine administration can cause falsely low test results.
Baxter Healthcare is recalling 31,130 bags of Fluconazole Injection due to potential leaks from incomplete seals, which may compromise sterility.
Beckman Coulter is recalling Lactate Assay kits because N-acetyl cysteine (NAC) administration can cause falsely low test results.
Beckman Coulter is recalling Cholesterol Assay kits because N-acetyl cysteine administration can cause falsely low results.
Siemens Medical Solutions is recalling 50 Syngo.plaza PACS systems because images may be lost if the system crashes before saving data to the hard disk.