The Recall Desk

State

Nebraska product recalls

72,971 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.

These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6026–6050 of 77518

  • SevereNHTSA·25V395000·2025-07-23

    BMW electric drive motor software can shut down high voltage system

    BMW is recalling certain 2022-2025 i4, 2022-2024 iX, 2023-2024 i7 and 2024 i5 vehicles because electric drive motor software may shut down the high-voltage system, causing a loss of drive power.

    Product
    BMW — BMW I5, IX, I4, I7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V481000·2025-07-23

    Tiffin motorhome alternator programming error can stall the engine

    Tiffin is recalling certain 2023-2026 motorhomes with 2.0 litre engines because the secondary alternator controller programming was not properly updated, which can stall the engine.

    Product
    TIFFIN — TIFFIN GH2, CONVOY, GH1, GT1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0305-2025·2025-07-23

    Dubai emek pistachio cacao spread may be contaminated with Salmonella

    Dubai emek Spread Pistachio Cacao Cream with Kadayif is being recalled after the FDA notified the firm that the product may be contaminated with Salmonella. 316 cases are affected.

    Product
    Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz UPC 8 69652 10130 1 Manufacturer: Emek Dogal Saglik Urunlerilkl. Gida Turkey
    Category
    Food
    Distribution
    32 states
  • HighFDA (Drugs)·D-0519-2025·2025-07-23

    Levothyroxine sodium 25 microgram bottles of 1000 assayed below specification

    Levothyroxine Sodium Tablets, USP 25 mcg in 1000-count bottles from Accord Healthcare are being recalled because the product is subpotent. 2,352 bottles are affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0525-2025·2025-07-23

    Omeprazole capsule bottle contained a foreign divalproex sodium tablet

    Omeprazole Delayed-release Capsules USP 20 mg are being recalled because a foreign Divalproex Sodium Extended-Release 250 mg tablet was found in a bottle. 1,476 bottles affected.

    Product
    OMEPRAZOLE — OMEPRAZOLE (OMEPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2122-2025·2025-07-23

    VITROS CHE slides can cause quality control drift with performance verifiers

    VITROS Chemistry Products CHE Slides are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.

    Product
    VITROS Chemistry Products CHE Slides; Catalog Numbers: (1) 191 4605 (300 slides), (2) 800 4707 (90 slides);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2118-2025·2025-07-23

    NIO-A intraosseous device stabilizer may not release properly after insertion

    The NIO-A NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 7,056 US units affected.

    Product
    Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000603 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intra-osseous access device supplied Sterile and single use. Indicated for Intra-osseous access t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0533-2025·2025-07-23

    Rizatriptan 5 mg tablets exceed the acceptable intake limit for nitrosamine

    Rizatriptan Benzoate Tablets USP 5 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.

    Product
    RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2123-2025·2025-07-23

    VITROS CHE slides sold in Japan can cause quality control drift

    VITROS Chemistry Products CHE Slides supplied in Japan are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.

    Product
    VITROS Chemistry Products CHE Slides (Japan); Catalog Numbers: (1) 684 4074 (90 slides), (2) 684 4138 (300 slides);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0518-2025·2025-07-23

    Levothyroxine sodium 25 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 25 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 82,159 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0523-2025·2025-07-23

    Levothyroxine sodium 150 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 150 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 4,921 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0289-2025·2025-07-23

    Fudge Frenzy bars recalled over potential Listeria monocytogenes contamination

    Fudge Frenzy Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Fudge Frenzy Bar (86210), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0295-2025·2025-07-23

    YoCrunch vanilla yogurt with Oreo pieces may contain plastic material

    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Oreo cookie pieces, is being recalled because of foreign material in the form of plastic.

    Product
    YoCrunch Low Fat Yogurt with toppers. Vanilla with Oreo cookie pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00080 2. Multipack containing 4-4 oz. cups UPC 46675-01350 Keep Refrigerated. Distributed by Danone US, LLC, White
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0286-2025·2025-07-23

    Rich Bar frozen novelties recalled over potential Listeria monocytogenes contamination

    Rich Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Rich Bar (85155), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Drugs)·D-0522-2025·2025-07-23

    Levothyroxine sodium 112 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 112 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 4,896 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0296-2025·2025-07-23

    YoCrunch vanilla yogurt with Snickers pieces may contain plastic pieces

    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00112 2. Multipack containing 4-4 oz. cups UPC 46675-01326 Keep Refrigerated. Distributed by Danone US, LLC, White Pla
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0287-2025·2025-07-23

    Crumbled cookie bars recalled over potential Listeria monocytogenes contamination

    Crumbled Cookie Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Crumbled Cookie Bar (85200), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighNHTSA·25V482000·2025-07-23

    Hyundai IONIQ 5 battery bus bar may be improperly tightened

    Hyundai is recalling certain 2025 IONIQ 5 vehicles because the high voltage battery may contain an improperly tightened bus bar that can short circuit. Owners are told to park outside until repaired.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2112-2025·2025-07-23

    BLS laser show projectors shipped without a working remote interlock connector

    BLS laser light show projectors, models CLUB 1000, 2000 and 4000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 12 units affected.

    Product
    Laser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000.
    Category
    Other
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0290-2025·2025-07-23

    Cotton Candy Twirl bars recalled over potential Listeria monocytogenes contamination

    Cotton Candy Twirl Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Cotton Candy Twirl Bar (86260), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Devices)·Z-2113-2025·2025-07-23

    BLS PURE laser projectors shipped without a working remote interlock connector

    BLS laser light show projectors, models PURE 5000 and PURE 10000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 3 units affected.

    Product
    Laser light show projectors manufactured by BLS, Model PURE 5000/10000.
    Category
    Other
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0524-2025·2025-07-23

    Levothyroxine sodium 175 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 175 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 2,344 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0532-2025·2025-07-23

    Lisinopril and hydrochlorothiazide bottle contained a foreign antiretroviral tablet

    Lisinopril and Hydrochlorothiazide Tablets 20 mg/12.5 mg are being recalled after a complaint that a sealed bottle contained a foreign tablet identified as atazanavir and ritonavir. 58,968 bottles affected.

    Product
    LISINOPRIL AND HYDROCHLOROTHIAZIDE — LISINOPRIL AND HYDROCHLOROTHIAZIDE (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0284-2025·2025-07-23

    Chocolate crunch cake bars recalled over potential Listeria monocytogenes contamination

    Chocolate Crunch Cake Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Chocolate Crunch Cake Bar (85000), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states