State
73,088 recalls have nationwide distribution and so reach Nebraska. 4,575 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,575 recalls naming Nebraska we have scored against our rubric, 715 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,131 (25%) are Severe.
Which agencies issued them
These figures cover only the 4,575 recalls whose distribution notice names Nebraska specifically. The 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
JR Watkins Cooling Pain Relief Patches are being recalled due to manufacturing process deviations identified during production.
Medline is recalling Endo Kit models containing Olympus components with missing sterile and manufacturing lot numbers and expiration dates on packaging. Without this labeling, medical facilities cannot verify product expiration or track inventory.
FDA recalls THERA CARE COLD HOT MEDICATED PATCH (menthol 5%) due to manufacturing practice deviations. The voluntary recall affects 279,936 patches distributed nationwide.
Abbott is recalling 130 Merlin@home cardiac transmitters that cannot update software after power interruption during firmware download. Affected devices remain on outdated firmware with no ability to receive future updates.
Water condensation may accumulate under the autosampler's thermal insulation and damage the main board, causing communication errors and delays in laboratory testing. Two Shimadzu models are affected: SIL-40C XR CL and SIL-40C X3 CL.
Unexo Life Sciences Private Limited is voluntarily recalling Parche Leon pain relief patches due to manufacturing practice deviations. No illnesses or injuries have been reported.
GE Healthcare is recalling certain Proteus XR/A radiographic systems because steel cables in the Wall Stand component have not been replaced at manufacturer-specified maintenance intervals.
Unexo Life Sciences is recalling Absorbine Jr Pain Relieving Knee Patch nationwide due to manufacturing process deviations that do not meet FDA standards. No illnesses or injuries have been reported.
Equate Maximum Strength Lidocaine Pain Relieving Patches (4%) are being recalled due to current Good Manufacturing Practice deviations. Approximately 1.1 million patches were distributed nationwide in the US.
J.R. Watkins is recalling Cooling Menthol Extra Strength Pain Relief Patches nationwide due to manufacturing practice deviations. The recall affects approximately 7,138 patches from lots JC101, JC102, and JC103.
THERACARE MAXIMUM STRENGTH PAIN RELIEF PATCH (4% lidocaine) is being recalled nationwide due to manufacturing practice deviations. Unexo Life Sciences, the manufacturer, voluntarily initiated the recall after identifying quality control issues.
Remote Diagnostic Technologies Ltd. is recalling Tempus LS-Manual Defibrillator Model 00-3020 units distributed in eight U.S. states. The devices were labeled incorrectly during servicing with wrong product name and CAT number.
PACCAR is recalling 2025 Kenworth T880 and other commercial vehicles due to steering arm and tie rod bracket fasteners that may fail, resulting in loss of steering control and increased crash risk.
Nova Bus recalled 2022-2024 LFS buses for incorrectly installed wheelchair securement systems. The attachment points may be in wrong locations, preventing proper restraint in crashes.
International is recalling 2025 EMV vehicles because a missing circuit breaker may cause the windshield defrosting system to fail, reducing visibility.
Pierce is recalling 2023-2024 Velocity, Enforcer, and Quantum fire trucks because front steer axle tires are incompatible with the wheels, increasing crash risk.
Tesla is recalling 2024 Model X vehicles because flickering parking lights and low beam headlights may fail to sufficiently illuminate the roadway, increasing crash risk.
PACCAR is recalling 2024-2025 Kenworth and Peterbilt commercial trucks with insufficient axle bearing lubrication, which may cause wheel hub overheating and fire or loss of vehicle control.
Kuntry Kustom RV is recalling 2023-2024 Rich Specialty Sanitation and Office trailers because a faulty air conditioner component may overheat and cause a fire.
McLaren is recalling 163 2021 765LT Coupe vehicles because the rear cabin window may detach due to insufficient adhesive bonding, creating a road hazard.
Baxter Healthcare Corporation is recalling 1,240 units of MiniCap Extended Life PD Transfer Sets (Part Number T5C4484) due to potential exposure to polychlorinated biphenyls and related compounds when used in peritoneal dialysis treatments.
Baxter MiniCap Extended Life PD Transfer Sets (Part 5C4482S) are being recalled due to potential exposure to polychlorinated biphenyls (PCBs). The FDA Class I recall affects 151,020 units distributed worldwide.
Counterfeit CSB batteries are being used in Plum Infusion Systems. These unauthorized batteries fail to hold their charge and have not been tested for use with the pumps.
Chrysler is recalling 2017-2018 Ram 2500, 3500, 4500, and 5500 trucks because the hydraulic control unit may fail, disabling anti-lock brakes and stability controls.
Chrysler is recalling certain 2022-2024 Grand Cherokee and 2021-2024 Grand Cherokee L vehicles because an improperly secured connector may prevent the front seat side airbags deploying. All units have been remedied.