The Recall Desk

State

Nebraska product recalls

72,984 recalls have nationwide distribution and so reach Nebraska. 4,547 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,547
Critical
705
Severe
1,119
Most recent
2026-09-09

Of the 4,547 recalls naming Nebraska we have scored against our rubric, 705 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,119 (25%) are Severe.

Which agencies issued them

These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7076–7100 of 77531

  • ModerateFDA (Devices)·Z-1578-2025·2025-04-23

    Rover Mobile X-ray System Recalled for Potential Early Tube Failure

    Micro-X Ltd. is recalling 31 Rover Mobile X-ray Systems (Model MXU-RV71) due to potential early life failure of the x-ray tube caused by excessive thermal load on the anode. The systems were distributed nationwide in California, New Jersey, and Puerto Rico.

    Product
    Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contained X-ray generator, imaging display and software for acquiring medical diagn
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1571-2025·2025-04-23

    ID NOW COVID-19 2.0 Point-of-Care Test Device Recall

    Abbott is recalling certain lots of the ID NOW COVID-19 2.0 24T test device due to higher invalid result rates than stated in product instructions. The affected lots were distributed worldwide.

    Product
    Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-000 Software Version: N/A Product Description: Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1577-2025·2025-04-23

    Maquet VH-3010 Power Supply Recalled for Inadequate Heating Function

    Maquet Cardiovascular is recalling 110 units of the VH-3010 Power Supply due to an incorrect resistor that may prevent the HemoPro 2 harvesting tool jaws from heating adequately.

    Product
    Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0366-2025·2025-04-23

    Chlorpromazine Hydrochloride Tablets Recalled Due to Impurity

    The FDA is recalling Chlorpromazine Hydrochloride Tablets, 10 mg, due to the presence of N-Nitroso-Desmethyl Chlorpromazine impurity above recommended limits. The affected lot was distributed nationwide.

    Product
    ChlorproMAZINE Hydrochloride Tablets, USP, 10 mg, packaged in cartons of 100 TABLETS (10x10), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7129-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1587-2025·2025-04-23

    Medline Convenience Kits Rhinoplasty Pack Potential Weak Seals Recall

    Medline Industries is recalling Rhinoplasty Pack convenience kits (Model DYNJ84116A, Lot 24IBH580) due to potential open or weak seals on breather pouches used for packaging. Compromised packaging may affect sterility of the sterile kits.

    Product
    Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK, Model Number: DYNJ84116A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1606-2025·2025-04-23

    Medline Convenience Kit Skin Lesion Set Potential Seal Defect

    Medline is recalling its Skin Lesion Set convenience kits due to potential open or weak seals on breather pouches used for packaging. The compromised seals may affect the sterility of the kits.

    Product
    Medline Convenience kits used for various procedures: 1) SKIN LESION SET, Model Number: MNS6270
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V271000·2025-04-23

    Ford Recalls 2025 F-150 Vehicles for Missing Air Bag Warning Labels

    Ford is recalling 2025 F-150 vehicles because the air bag warning label may be missing from the dashboard, failing to comply with federal safety standards.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1602-2025·2025-04-23

    Sterile convenience kits recalled for potentially weak breather pouch seals

    Medline Industries is recalling sterile convenience kits due to potential open or weak seals on breather pouches used in packaging. Defective seals may compromise product sterility.

    Product
    Refer to RES
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1572-2025·2025-04-23

    ID NOW Influenza A/B 2 24T Diagnostic Assay Invalid Result Rates

    Abbott Diagnostics is recalling certain lots of the ID NOW Influenza A/B 2 24T diagnostic assay due to higher-than-expected invalid test result rates. Affected lots were distributed worldwide.

    Product
    Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software Version: N/A Product Description: Influenza A And Influenza B Multiplex Nucleic Acid Assay; Real Time Nucleic Acid Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1609-2025·2025-04-23

    Medline Hernia Repair Convenience Kit Recalls Due to Weak Seals

    Medline is recalling Hernia Repair Tote convenience kits (Model DYNJ908337C) because purchased breather pouches used for packaging may have open or weak seals, which could compromise product sterility.

    Product
    Medline Convenience kits used for various procedures: 1) HERNIA REPAIR TOTE, Model Number: DYNJ908337C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0705-2025·2025-04-23

    Dried Seedless Plum Candy Recalled Due to Undeclared Cyclamates

    BaiWei ShanZhuang Dried Seedless Plum Candy is being recalled because it contains cyclamates, which are not declared on the label. The product was distributed across multiple states.

    Product
    BaiWei ShanZhuang, Dried Seedless Plum Candy, 9.16 oz. (260g), plastic bags, 30 bags per case.
    Category
    Food
    Distribution
    11 states
  • SevereNHTSA·25V266000·2025-04-22

    IC school bus driver seat belt anchor bolts may come loose

    International is recalling certain 2025-2026 IC CESB and 2025 EVSB school buses because the driver's seat belt anchor bolt may come loose, so the belt may not restrain the driver in a crash.

    Product
    IC BUS — IC BUS CESB, EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V268000·2025-04-22

    Utilimaster Aeromaster Recall for Improperly Tightened Seat Fasteners

    Shyft Group is recalling 2022-2025 Utilimaster Aeromaster vehicles because suspension seat mounting fasteners may be improperly tightened, increasing injury risk in a crash.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25C006000·2025-04-22

    Dorel Safety 1st Child Seat Recall for Loose Headrest Foam

    Dorel Juvenile Group is recalling Safety 1st Grow & Go Sprint child seats because the headrest foam pad is not adequately secured, posing a choking hazard.

    Product
    CHILD SEAT:MATERIAL/PADDING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V262000·2025-04-21

    Motiv Recalls 2020 F-59 School Buses Due to Power Bracket Defect

    Motiv Power Systems is recalling 2020 F-59 BEV chassis school buses because a support bracket may break, causing an electrical short and loss of drive power.

    Product
    MOTIV — MOTIV F-59 BEV CHASSIS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V265000·2025-04-21

    Highland Ridge Recalls 2025 GO Play Travel Trailers for Label Errors

    Highland Ridge RV is recalling 2025 GO Play travel trailers because incorrect weight and tire labels may lead to overloading and crashes.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT GO PLAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04192025-01·2025-04-19

    Cargill Pork Carnitas Recalled for Possible Metal Contamination

    USDA FSIS issued a public health alert for Cargill pork carnitas potentially contaminated with metal pieces. No injuries have been reported.

    Product
    Cargill Meat Solutions — FSIS Issues Public Health Alert for Pork Carnitas Products Due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V261000·2025-04-18

    Motiv Recalls F-53 and F-59 Chassis Due to Bracket Failure Risk

    Motiv Power Systems is recalling 2019-2022 F-53 and F-59 chassis vehicles because a support bracket may break, causing an electrical short and loss of drive power.

    Product
    MOTIV — MOTIV F-53 BEV CHASSIS, F-59 BEV CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V263000·2025-04-18

    Motorhome slide-room floor may not retain seat belts in a crash

    Forest River is recalling certain 2025 East to West Bravado BRC33DSF motorhomes because the slide-room floor may detach in the open position and may not properly retain the seat belts during a crash.

    Product
    EAST TO WEST — EAST TO WEST BRAVADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V264000·2025-04-18

    Forest River trailer accent lights and awning wiring lack circuit protection

    Forest River is recalling certain 2024-2025 Aurora and Coachmen Catalina travel trailers because the front accent lights, awning and auto-levelling system may be incorrectly wired without overcurrent protection.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN AURORA, CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V250000·2025-04-17

    Altec Recalls 2014-2016 AT200A Aerial Devices Due to Frame Cracks

    Altec is recalling 2014-2016 AT200A aerial devices because cracks in the mounting frame legs may cause the side plate to break, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V257000·2025-04-17

    Volvo truck idler gear can detach from the engine causing stall

    Volvo Trucks is recalling certain 2022-2025 VN and 2025 New VN trucks because improperly tightened idler gear bracket fasteners may allow the idler gear to detach from the engine.

    Product
    VOLVO — VOLVO VNL (4), VN
    Category
    Vehicle
    Distribution
    Distributed nationwide