The Recall Desk

State

Nebraska product recalls

73,737 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,580
Critical
713
Severe
1,345
Most recent
2026-10-28

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.

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.

35076–35100 of 78317

  • SevereNHTSA·19V572000·2019-08-02

    Mercedes-Benz Recalls 2020 GLE Models Due to Fuel Tank Weld Defect

    Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because an improper weld on the fuel filler pipe may cause a fuel leak, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V571000·2019-08-02

    Mercedes-Benz Recalls SL Models for Passenger Air Bag Seam Defect

    Mercedes-Benz is recalling certain 2018-2019 SL models because the front passenger air bag seam may tear during deployment, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SL 550, AMG SL65, AMG SL63, SL 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V567000·2019-08-01

    Toyota Recalls 2019 Camry Vehicles for Air Bag Calibration Defect

    Toyota is recalling 2019 Camry vehicles because the occupant classification system may be improperly calibrated, potentially preventing front passenger air bags from deploying in a crash.

    Product
    TOYOTA — TOYOTA CAMRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V569000·2019-08-01

    Honda Recalls 2019 CR-V Vehicles for Fuel Tank Weld Defect

    Honda is recalling 2019 CR-V vehicles because an insufficient weld on the fuel tank may cause fuel leaks, increasing the risk of fire.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V568000·2019-08-01

    Winnebago Recalls 2018-2019 Fuse Motorhomes Due to Wheel Stud Defect

    Winnebago is recalling 2018-2019 Fuse motorhomes because wheel studs may be too long, preventing lug nuts from securing wheels properly and increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO FUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V566000·2019-08-01

    Thor Motor Coach Recalls 2019-2020 Omni and Magnitude Motorhomes

    Thor Motor Coach is recalling 2019-2020 Omni and Magnitude motorhomes because the battery tray may detach, causing the vehicle to stall.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH MAGNITUDE, OMNI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1966-2019·2019-07-31

    Probar Meal Original Trail Mix Recalled for Undeclared Milk and Soy

    Probar LLC is recalling 14,999 bars of PROBAR MEAL Original Trail Mix because they may contain undeclared milk and soy allergens.

    Product
    PROBAR MEAL Original Trail Mix, Net Wt. 3oz. (85g), Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalCPSC·19177·2019-07-31

    Dorel Recalls Inclined Infant Sleepers Due to Suffocation Risks

    Dorel Juvenile Group is recalling about 24,000 inclined infant sleepers, including Eddie Bauer and Disney Baby models, due to safety concerns about inclined sleep products.

    Product
    Eddie Bauer Slumber and Soothe Rock Bassinet; Disney Baby Doze and Dream Bassinet
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2056-2019·2019-07-31

    Top Chef Meals Grilled Bison Burger Recalled for E. coli Contamination

    The Crystal Spoon Corp. is recalling Top Chef Meals Grilled Bison Burgers due to potential E. coli contamination. Consumers should not eat the product.

    Product
    Top Chef Meals Grilled Bison Burger best used by date between 5/4/19-6/30/19 Unit Size: 6 and 8 oz sizes Container Description: Plastic PETE dual ovenable No specific UPC number
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1507-2019·2019-07-31

    Pharma-Natural Recalls Workvie Pain Roll-On for Manufacturing Violations

    Pharma-Natural Inc. is recalling Workvie Instant Pain Relieving Roll On due to current good manufacturing practice deviations, including lack of process and cleaning validation.

    Product
    Workvie Instant Pain Relieving Roll On (Lidocaine HCL 4% + Menthol 1% & Arnica), 2.5oz (71 g) roll on bottle, Exclusively Distributed by: Marketite, LLC., Coral Gables, FL 33134, NDC 72393-201-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1587-2019·2019-07-31

    Brand Castle Recalls Hot Cocoa Cookie Mix Due to E. coli Risk

    Brand Castle LLC is recalling Hot Cocoa Cookie Mix because a supplier reported potential E. coli contamination in the flour used.

    Product
    Hot Cocoa Cookie Mix, 22.9 oz glass jar, 6/case
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-1584-2019·2019-07-31

    Brand Castle Brownie Mix Recalled for Potential E. coli Contamination

    Brand Castle LLC is recalling Billion Dollar Brownie Mix due to potential E. coli contamination in flour. The product was distributed in ten states.

    Product
    Billion Dollar Brownie Mix, 28.3 oz glass jar, 6/case
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-1528-2019·2019-07-31

    Gordon Laboratories Recalls MONSEL'S Solution Due to Microbial Contamination

    Gordon Laboratories is recalling 277 boxes of MONSEL'S (Ferric Subsulfate) Solution due to microbial contamination and high iron content.

    Product
    MONSEL'S (Ferric Subsulfate) Solution, 8 mL amber glass bottle, packaged as one dozen bottles with applicators per box, Rx only, Gordon Laboratories, Upper Darby, PA 19082, NDC 10481-0112-8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1517-2019·2019-07-31

    Tris Pharma Recalls Hydrocodone and Chlorpheniramine Suspension Due to Potency Issues

    Tris Pharma is recalling 2,550 bottles of Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release Suspension due to high out-of-specification results for active ingredients and preservatives.

    Product
    HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX — HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX (HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1522-2019·2019-07-31

    Geritrex Recalls Gericare Diocto Liquid Stool Softener Due to Microbial Contamination Risk

    Geritrex, LLC is recalling 6,165 bottles of Gericare Diocto Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.

    Product
    Gericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg/5mL, 16 FL OZ (473 ml), Dist. BY: Gericare Pharmaceuticals corp. 1650 63rd Street Brooklyn, NY 11204, NDC 57896-403-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1967-2019·2019-07-31

    PROBAR Meal Wholeberry Blast bars recalled for potential undeclared milk and soy allergens

    The FDA is recalling PROBAR Meal Wholeberry Blast bars because they may contain undeclared milk and soy ingredients. Consumers should discard affected bars and consult their healthcare provider if allergic.

    Product
    PROBAR MEAL Wholeberry Blast, Net Wt. 3oz.(85g), Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1525-2019·2019-07-31

    Geritrex Recalls Ritussin DM Due to Potential Microbial Contamination

    Geritrex, LLC is recalling Ritussin DM Double Strength cough syrup due to cGMP deviations that may result in microbial contamination.

    Product
    Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V563000·2019-07-31

    BMW Recalls 2018-2019 X3 and X4 Models for Seatback Welding Defect

    BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because improperly welded front seatback frames may fold unexpectedly, increasing injury risk in a crash.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1524-2019·2019-07-31

    Geritrex Recalls Iron Elixir Due to Potential Microbial Contamination

    Geritrex, LLC is recalling Preferred Plus Pharmacy Iron Elixir due to cGMP deviations that may result in microbial contamination.

    Product
    Preferred Plus Pharmacy Iron Elixir Ferrous Sulfate, 220 mg, 16 fl oz. (473 mL), Distributed by: Geri-care Pharmaceuticals Corp. 1650 63rd Street Brooklyn, NY 11204, NDC 52807-177-16
    Category
    Drug
    Distribution
    Distributed nationwide