State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Herbal Doctor Remedies is recalling Thyro-Lo 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Ortho Clinical Diagnostics is recalling 2,531 VITROS 5600 Integrated Systems due to a software anomaly that may cause unsuccessful calibration.
Herbal Doctor Remedies is recalling Asma Stopper Capsules because they were manufactured outside of current Good Manufacturing Practice controls.
Polymer Technology Systems is recalling 559 vials of IVD Lipid Panel test strips because the accompanying MEMo chips may be mislabeled, potentially causing the analyzer to display the wrong lot number.
Polymer Technology Systems is recalling Lipid Panel test strips because the included MEMo chips may display the wrong lot number on the analyzer screen.
Sage Products Inc is voluntarily recalling a lot of Independent Care System kits because the included Sodium Bicarbonate Mouthpaste tubes may be cosmetically damaged.
SunSetter is recalling vinyl covers for motorized awnings because they can cause unexpected opening and falls. One death and six injuries have been reported.
Tiffin is recalling 2019-2020 Allegro Open Road motorhomes because a hydraulic hose may rub against the tire, causing sudden deflation and crash risk.
E-One is recalling 2019 Cyclone II and Typhoon fire trucks because air bag cushions may detach and fail to inflate during a crash.
Kia is recalling 2020 Telluride vehicles because seat belt assemblies may not securely hold child restraints in a crash, increasing injury risk.
VanLeigh is recalling 2015-2019 Beacon and Vilano fifth wheel trailers because short suspension shackles may fail, increasing crash risk.
Mercedes-Benz is recalling 2020 GLE and GLS vehicles because incorrectly installed air conditioner drain hoses may cause water to enter the cabin, increasing the risk of fire.
Ford is recalling 2015 Fusion and Lincoln MKZ vehicles because heat from seat belt pretensioners may cause anchor cables to fail, increasing injury risk in crashes.
Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because the rear middle seatbelt anchor may be loose, increasing injury risk in a crash.
Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because taillights may dim or turn off if the turn switch is moved quickly, increasing crash risk.
BMW is recalling 2020 745e xDrive vehicles because a software error may disable the audible seat belt warning for the driver, increasing injury risk in a crash.
Mercedes-Benz is recalling 2018-2019 C300 and C43 AMG vehicles because the 12-volt battery bracket may be unsecured, risking terminal disconnection in a crash.
Mercedes-Benz is recalling one 2019 S 450 vehicle because improperly installed pillar covers may prevent side curtain air bags from deploying correctly during a crash.
Dennis Eagle is recalling one 2017 Diego vehicle because a switch failure may cause instrument controls to move sides and disable the electronic braking system.
Forest River is recalling 2020 Columbus Fifthwheel Trailers because the rear ladder blocks the egress window, preventing emergency exit.
Navistar is recalling 2,677 IC school buses because the roof hatch external handle may break, preventing emergency egress.
Navistar is recalling 2019-2020 IC RE and IC CE commercial buses because the roof hatch external handle may break, potentially preventing emergency egress.
ImprimisRx NJ is recalling 246 bottles of Timolol-Dorzolamide-Latanoprost ophthalmic drops because the medication was found to be subpotent.
Qiagen Sciences LLC is recalling specific lots of Filter-Tips used with QIAsymphony instruments because a small percentage of tips are leaking.
LNK International is recalling specific lots of Equate Nighttime Sleep Aid because of microbial contamination in the non-sterile product.