State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer Manufacturing B.V. is recalling 400 units of Trilogy Acet Shell hip implant components due to insufficient sealer calibration data.
Zimmer Manufacturing B.V. is recalling 1,220 units of Versus hip implants due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Zimmer Manufacturing B.V. is recalling 13 Versys Cemented Femoral Stems due to insufficient sealer calibration data. The affected sterile products were distributed nationwide in the US.
Zimmer Manufacturing B.V. is recalling 3,415 sterile compression screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Zimmer Manufacturing B.V. is recalling NexGen All-Poly Patella and related knee arthroplasty components due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Zimmer Manufacturing B.V. is recalling 154 sterile bone fixation screws distributed nationwide due to insufficient sealer calibration data.
Zimmer Manufacturing B.V. is recalling sterile intramedullary fixation rods and lag screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Zimmer Manufacturing B.V. is recalling specific sterile bone fixation screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Zimmer Manufacturing B.V. is recalling 512 sterile I/B II Knee Domed Patella components for total knee arthroplasty due to insufficient sealer calibration data.
Zimmer Manufacturing B.V. is recalling specific sterile orthopedic fixation devices due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Zimmer Manufacturing B.V. is recalling 119 sterile bone fixation appliances due to insufficient sealer calibration data. The affected products were packaged between August 2010 and April 2013.
Zimmer Manufacturing B.V. is recalling specific distal femoral components used in total hip arthroplasty due to insufficient sealer calibration data.
Teva Pharmaceuticals USA is recalling 576 bottles of Nabumetone 750 mg tablets because they lack required leaflets and approved labels.
Pharmedium Services, LLC is recalling specific lots of repinephrine bitartrate injection bags due to subpotency and discoloration confirmed by FDA analysis.
Forest River is recalling 2016 Cherokee Grey Wolf recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which may lead to overloading and tire blowouts.
Weiler is recalling 368 trucks from 2002-2016 because LED marker lights lack required reflectors, reducing visibility and increasing crash risk.
Triumph is recalling 2016 Street Twin motorcycles because damaged wiring insulation may allow fuel to leak, increasing the risk of fire.
Winnebago is recalling 2016 Winnie Drop trailers because the refrigerator compartment may not seal properly, allowing carbon monoxide to enter the cabin.
Subaru is recalling 2015-2016 Forester and WRX vehicles because a cracked turbocharger air intake duct may cause engine stalls, increasing crash risk.
Panasonic is recalling specific lithium-ion battery packs for CF-S10 Series laptops because a manufacturing defect poses a fire risk. No injuries have been reported.
RacerMate is recalling approximately 25,000 CompuTrainer Blue Flywheels because they can shatter during use, posing a risk of injury to riders and bystanders.
General Motors is recalling 2014-2016 Chevrolet Caprice Police Pursuit vehicles because corrosion may cause loss of electric power steering assist, increasing crash risk.
IKEA is recalling about 30,600 Gothem floor and table lamps because damaged cables can contact the metal body, posing a shock hazard. Consumers should stop using the lamps and return them for a full refund.
International Specialty Services is recalling Evercraft jack stands sold by NAPA Auto Parts because improper welds may cause the stands to collapse, posing an injury risk.
Rosenbauer is recalling 2012-2015 Commander vehicles because brake pedal pistons may corrode, making brakes difficult to activate or causing them to drag.