The Recall Desk

State

Nebraska product recalls

73,100 recalls have nationwide distribution and so reach Nebraska. 4,575 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,575
Critical
715
Severe
1,131
Most recent
2026-09-23

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.

These figures cover only the 4,575 recalls whose distribution notice names Nebraska specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10451–10475 of 77675

  • ModerateFDA (Devices)·Z-2697-2024·2024-08-28

    Medline Medical Soft Liner Recall Due to Dimensional Variation

    Medline Industries recalls 1.5L medical soft liners due to slight dimensional variations that may cause difficulty fitting into the outer canister. The recall affects 88,703 units distributed worldwide.

    Product
    1,5L MED-SOFT LINER W/ 6MMX1,8M TUB. & ADULT VC, REF OR53926
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2708-2024·2024-08-28

    Medline Medical Procedure Kits Recalled for Dimensional Variation in Canister Fitting

    Medline Industries is recalling 75,098 medical procedure kits due to slight dimensional variations that may cause difficulty fitting into their outer canisters. No injuries or illnesses have been reported.

    Product
    Medline medical procedure kits labeled as follows: a) AAA CDS, REF CDS984011C; b) CAN KIT, REF DYKM1184; c) DENTAL CDS, REF CDS984010B; d) EGD KIT, REF DYK1253578F; e) EGD REG KIT, REF DYKE1830; f) ENDO KIT, REF DYKE1516A; g) ERCP REG KIT, REF DYKM2127; h) GI P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2696-2024·2024-08-28

    Medline Soft Liner Dimensional Variation May Affect Outer Canister Fit

    Medline Industries is recalling 1500ML soft liners due to dimensional variations that may make fitting into the outer canister more difficult. No injuries have been reported.

    Product
    1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2699-2024·2024-08-28

    Medical Device Liner Recalled for Dimensional Variation Affecting Fit

    Medline Industries has recalled 316,125 units of its MED-SOFT Single Liner with Solidifier due to a dimensional variation that may cause difficulty when inserting the product into the outer canister.

    Product
    1,5L MED-SOFT SINGLE LINER WITH SOLIDIFIER, REF OR1920PG
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2713-2024·2024-08-28

    Medline Medical Procedure Kits Recalled for Dimensional Variation Affecting Outer Canister Fit

    Medline Industries is recalling certain C-Section surgical kits due to dimensional variations that could cause difficulty fitting into the outer canister. The recall affects 1,753 units distributed worldwide.

    Product
    Medline medical procedure kits labeled as follows: a) C-SECTION CDS, REF CDS983998C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2639-2024·2024-08-28

    C-Flow Bag Decanter Packaging Defects Prompt Sterile Barrier Recall

    Microtek Medical Inc. recalls C-Flow Bag Decanters (10,366 cases) due to pin holes and tears in sterile barrier packaging discovered during quality testing. The defects could allow bacterial contamination.

    Product
    C-Flow Bag Decanter, REF 2000S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0642-2024·2024-08-28

    FDA recalls Timolol Maleate eye drops due to defective bottle cap

    FDC Limited recalls Timolol Maleate Ophthalmic Solution nationwide because the bottle cap spike becomes lodged in the nozzle, preventing patients from dispensing the medication. No illnesses have been reported.

    Product
    TIMOLOL MALEATE — TIMOLOL MALEATE (TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2707-2024·2024-08-28

    Medline Medical Procedure Kits Recalled for Dimensional Variation

    Medline Industries recalled 3,539 medical procedure kits due to a dimensional variation that may prevent proper fitting into their outer storage canister. The FDA classified this as a Class II recall.

    Product
    Medline medical procedure kits labeled as follows: a) MAJOR BREAST, REF DYNJ905004C; b) MINOR BREAST, REF DYNJ905002B; c) SUCTION MEDI VAC, REF DYKM2033
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V641000·2024-08-27

    Jayco motorhome rearview camera image may not display

    Jayco is recalling certain 2023-2025 Entegra Ethos, Ethos LI, Arc, Jayco Swift, Swift LI and Comet motorhomes because radio software may prevent the rearview image from displaying, failing FMVSS 111.

    Product
    JAYCO — JAYCO, ENTEGRA SWIFT LI, ETHOS LI, ETHOS, COMET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V642000·2024-08-27

    Kentucky Trailer Recalls 2022-2024 MV and PV Truck Bodies for Floor Defect

    Kentucky Trailer is recalling 2022-2024 MV and PV truck bodies because the upper cargo floor may not be secured properly, allowing crossmembers to loosen and detach.

    Product
    KENTUCKY TRAILER — KENTUCKY TRAILER MV, PV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E072000·2024-08-26

    USK Internacional Recalls Tie Rod and Drag Link Assemblies

    USK Internacional is recalling certain tie rod and drag link assemblies due to improperly heat-treated ball studs that may break, potentially causing a loss of steering control.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V640000·2024-08-26

    Toyota Sequoia Hybrid tow hitch covers may come loose and detach

    Toyota is recalling certain 2023-2024 Sequoia Hybrid vehicles with a tow hitch cover attached to the rear bumper because the cover may come loose and detach from the vehicle.

    Product
    TOYOTA — TOYOTA SEQUOIA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V633000·2024-08-23

    Jaguar Recalls 2019 I-PACE Vehicles Due to High-Voltage Battery Overheating Risk

    Jaguar is recalling 2,760 2019 I-PACE vehicles because the high-voltage battery may overheat, increasing the risk of a fire. Owners should park outside and limit charging to 80% until repairs are complete.

    Product
    JAGUAR — JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V637000·2024-08-23

    Great Dane Recalls 2025 Everest SS Trailers Due to Welding Defect

    Great Dane is recalling 2025 Everest SS refrigerated trailers because improperly welded support gear bracing mounts may cause the trailer to collapse.

    Product
    GREAT DANE — GREAT DANE EVEREST SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E073000·2024-08-23

    Navico Recalls Progressive RV Surge Protectors Due to Ground Contact Defect

    Navico Group is recalling Progressive RSM-30 and PSK-30 surge protectors for recreational vehicles because the ground contact may fail, increasing the risk of electrical shock.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V634000·2024-08-23

    Ford fuel injectors assembled without O-ring support discs may leak

    Ford is recalling certain Lincoln Corsair, Escape, Mustang and Explorer vehicles because fuel injectors may have been assembled without O-ring support discs. 24 units affected.

    Product
    FORD — FORD, LINCOLN MUSTANG, ESCAPE, EXPLORER, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V635000·2024-08-23

    Ford EcoBoost engine intake valves may break while driving

    Ford is recalling certain 2021-2022 vehicles with 2.7L or 3.0L Nano EcoBoost engines because the engine intake valves may break, resulting in engine failure and loss of drive power.

    Product
    FORD — FORD, LINCOLN EDGE, BRONCO, NAUTILUS, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V628000·2024-08-22

    Forest River trailer tires may contact the outrigger and fail

    Forest River is recalling certain 2024 Salem and Wildwood travel trailers because the tire may contact the outrigger, causing the tire to fail. 34 units are affected.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24347·2024-08-22

    Head Rush Technologies TRUBLUE Speed Auto Belay Devices Fall Hazard

    Head Rush Technologies is recalling about 220 TRUBLUE Speed Auto Belay Devices because the backup brake can fail to activate, posing a fall hazard and risk of serious injury or death. Consumers should immediately stop using the devices and contact the manufacturer for a free inspection and repair.

    Product
    TRUBLUE Speed Auto Belay Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V629000·2024-08-22

    Salem and Wildwood trailer tires may contact chassis components and fail

    Forest River is recalling certain 2024-2025 Salem SBF325RL and Wildwood WBF325RL travel trailers because the tires may contact chassis components, causing tire failure.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide