The Recall Desk

State

Nebraska product recalls

73,817 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.

Which agencies issued them

These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49651–49675 of 78397

  • SevereFDA (Food)·F-2421-2016·2016-10-12

    Treehouse Foods Recalls Peanut Butter Dark Chocolate Protein Bars

    Treehouse Foods is recalling multiple brands of peanut butter dark chocolate protein bars due to potential contamination with Listeria monocytogenes from sunflower seeds.

    Product
    UPC 1373312015, Meijer Peanut Butter Dark Chocolate Protein Bars,Best By/Date Code: DEC 05 16, JAN 04 17. UPC 3225108607, Family Gourmet Peanut Butter Dark Chocolate Protein ,Bars Best By/Date Code: JAN 04 17. UPC 3680039453, Food Club Peanut Butter Dark Chocolate…
    Category
    Food
    Distribution
    38 states
  • SevereFDA (Food)·F-2525-2016·2016-10-12

    Rabbit Creek Brownie Mix Recalled Due to E. coli O121 Contamination

    Rabbit Creek Products Inc. is recalling Million Dollar Brownie Mix because it may contain flour contaminated with E. coli O121. Consumers should stop using the product.

    Product
    Million Dollar Brownie Mix, packaged in a plastic bag which is placed in a cardboard box, net wt. 12.7oz, UPC 010749011540
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2593-2016·2016-10-12

    Rabbit Creek Bread Mix Recalled for E. coli O121 Contamination

    Rabbit Creek Products is recalling Flower Pot Parmesan Southwest Beer Bread Mix because it may contain flour contaminated with E. coli O121.

    Product
    Flower Pot Parmesan Southwest Beer Bread Mix, packaged in a plastic bag which is placed in clay pot, net wt. 16.5oz, UPC 010749800823
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2409-2016·2016-10-12

    Treehouse Foods Recalls Sunflower Kernels for Listeria Contamination

    Treehouse Foods is recalling Nature's Harvest Sunflower Kernels, Ranch Flavored, due to potential contamination with Listeria monocytogenes.

    Product
    UPC 071725728074, Natures Harvest Sunflower Kernels Ranch Flavored, Best By/Date Code: 3/1/2017, 3/31/2017, 4/27/2017.
    Category
    Food
    Distribution
    38 states
  • SevereFDA (Food)·F-2452-2016·2016-10-12

    Treehouse Foods Recalls Nice! Peanut Lovers Trail Mix for Listeria Risk

    Treehouse Foods is recalling Nice! Peanut Lovers Trail Mix because it may contain sunflower seeds contaminated with Listeria monocytogenes.

    Product
    UPC 049022846524 Nice! Peanut Lovers Trail Mix., Best By/Date Code: 4/19/2017.
    Category
    Food
    Distribution
    38 states
  • SevereFDA (Food)·F-2572-2016·2016-10-12

    Rabbit Creek Caramel Pecan Quick Bread Mix Recalled for E. coli O121

    Rabbit Creek Products Inc. is recalling Caramel Pecan with Streusel Topping Quick Bread Mix because it may contain flour contaminated with E. coli O121.

    Product
    Caramel Pecan with Streusel Topping Quick Bread Mix, packaged in a plastic bag which is placed in a cardboard box, net wt. 18.25oz, UPC 010749008700
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2530-2016·2016-10-12

    Rabbit Creek Brownie Mix Recalled for E. coli O121 Contamination

    Rabbit Creek Products Inc. is recalling Raspberry with Cabernet Wine Brownie Mix because it may contain flour contaminated with E. coli O121.

    Product
    Raspberry with Cabernet Wine Brownie Mix, packaged in a plastic bag which is placed in a cardboard box, net wt. 10.8oz, UPC 010749040212
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2531-2016·2016-10-12

    Rabbit Creek Brownie Mix Recalled for E. coli O121 Contamination

    Rabbit Creek Products is recalling Redneck Brownie Mix because it may contain flour contaminated with E. coli O121.

    Product
    Redneck (Potato Chip & Bacon) Brownie Mix, packaged in a plastic bag which is placed in a cardboard box, net wt. 12oz, UPC 010749111165
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2436-2016·2016-10-12

    Treehouse Foods Recalls Nut Trail Mixes Due to Listeria Risk

    Treehouse Foods is recalling specific Amport Foods and Naturally Select nut trail mixes because they may contain sunflower seeds contaminated with Listeria monocytogenes.

    Product
    UPC 071725713124, Amport Foods Chocolatey Nut Trail Mix, Best By/Date Code: 1/8/2017 . UPC 639277431417, Naturally Select Chocolate & Nut Trail Mix, Best By/Date Code: 3/23/2017 .
    Category
    Food
    Distribution
    38 states
  • HighFDA (Devices)·Z-0015-2017·2016-10-12

    Siemens Recalls Ysio Max Radiographic Systems Due to Table Tilt Risk

    Siemens is recalling 37 Ysio Max radiographic systems because a table part may detach, causing the table to tilt and potentially injure patients.

    Product
    YSIO Max Product Usage: The Ysio Max is a radiographic system used in hospitals, clinics, and medical practices. Ysio Max enables radiographic and tomographic exposures of the whole body including: skull, chest, abdomen, and extremities and may be used on pediatric, adult…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2908-2016·2016-10-12

    Integra Drainage Accessory Kits Recalled Due to Incomplete Packaging Seal

    Integra LifeSciences Corp. is recalling specific lots of Integra Drainage Accessory Kits because a final inspection found an incomplete packaging seal, potentially compromising sterility.

    Product
    Integra Drainage Accessory Kits, REF 910122, Sterile EO, Rx only, packaged in one Tyvek pouch. Five (5) sealed Tyvek pouches are packaged in a cardboard box. Used for Intraoperative drainage of CSF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V732000·2016-10-12

    Coachmen Galleria Recalled for Incorrect Cargo Capacity Placard

    Forest River is recalling 2016-2017 Coachmen Galleria recreational vehicles because the cargo capacity placard is inaccurate, which may lead to overloading.

    Product
    COACHMEN — COACHMEN GALLERIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V730000·2016-10-12

    ShowHauler Garage Coach Lift Gate Chain Recall

    ShowHauler is recalling 2014-2015 Garage Coaches because lift gate roller chains may fail, causing the platform to drop and increasing injury risk.

    Product
    SHOWHAULER — SHOWHAULER GARAGE COACH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0013-2017·2016-10-12

    Siemens Recalls Multix Fusion X-Ray Systems Due to Table Tilt Risk

    Siemens is recalling 37 Multix Fusion X-ray systems because an internal table part may detach, causing the table to tilt and potentially injure patients.

    Product
    Multix Fusion Stationary X-Ray System Product Usage: The Multix Fusion system is a radiographic system used in hospitals, clinics, and medical practices. Multix Fusion enables radiographic exposures of the whole body including: skull, chest, abdomen and extremities and may…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0038-2017·2016-10-12

    RayStation Radiation Therapy Planning Software Recalled for Dose Calculation Errors

    RaySearch is recalling RayStation software versions 2.5 through 5.0 due to dose calculation errors when using specific region of interest settings.

    Product
    RayStation 2.5, 3.0, 3.5, 4.0, 4.5, 4.7, 5.0 and 4.3 (InverseArc 1.0) -- Radiation Therapy Treatment Planning System RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2905-2016·2016-10-12

    Integra Straight Ventricular Catheter Recalled for Incomplete Packaging Seal

    Integra LifeSciences Corp. is recalling 10 units of Straight Ventricular Catheters due to an incomplete packaging seal discovered during final inspection.

    Product
    Integra Straight Ventricular Catheter F8, 25 cm, Sterile EO, Rx only, packaged in a Tyvek pouch and secondary packaged in to Tyvek pouch, sealed in a cardboard box. Silicone elastomer Ventricular Catheter for use with hydrocephalus valves
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2909-2016·2016-10-12

    Integra Ventricular Catheter Accessory Kit Recalled for Incomplete Packaging Seal

    Integra LifeSciences Corp. is recalling 14 units of the Ventricular Catheter Accessory Kit due to an incomplete sterile packaging seal discovered during final inspection.

    Product
    Integra Ventricular Catheter Accessory Kit, REF 951303, Sterile EO, Rx only, packaged in a PVC tray, then secondary package in to Tyvek pouch and tertiary packaged in to Tyvek pouch. Sealed pouches are packaged in a cardboard box. F8 35cm Silicone Elastomer Ventricular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0039-2017·2016-10-12

    Siemens Dimension Vista Calcium Reagent Cartridge Recall for Erroneous Results

    Siemens Healthcare Diagnostics is recalling Dimension Vista Calcium reagent cartridges that may produce inaccurate test results.

    Product
    Dimension Vista¿ Calcium (CA) Flex¿ reagent cartridge Device Listing No.: D011443 Batch Number: 16060BB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0014-2017·2016-10-12

    Siemens Recalls Multix Fusion VA10 Radiographic Systems Due to Table Defect

    Siemens is recalling 37 Multix Fusion VA10 radiographic systems because a table part may detach, causing the table to tilt and potentially injure patients.

    Product
    Multix Fusion VA10 Product Usage: The Multix Fusion VA10 system is a radiographic system used in hospitals, clinics, and medical practices. Multix Fusion enables radiographic exposures of the whole body including:skull, chest, abdomen and extremities and may be used on…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0008-2017·2016-10-12

    Microgenics Recalls QMS Everolimus Assay Due to Reagent Stability Issue

    Microgenics Corporation is recalling the Thermo Scientific QMS Everolimus Assay because a reagent stability issue causes inaccurate test results for transplant patients.

    Product
    Thermo Scientific QMS Everolimus Assay; Model number: 0380000 (US Distribution); 0373852 (Foreign Distribution) Product Usage: The QMS Everolimus Assay is intended for the quantitative determination of Everolimus, in human whole blood on automated clinical chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17010·2016-10-12

    Mamas & Papas Recalls Armadillo Strollers Due to Fall Hazard

    Mamas & Papas is recalling Armadillo Flip and Flip XT strollers because a loose latch can cause the seat to tip back, posing a fall hazard to infants.

    Product
    Mamas & Papas Armadillo Flip Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V728000·2016-10-12

    Forest River Recalls 2017 Trailers Due to Air Conditioner Fire Risk

    Forest River is recalling 2017 Flagstaff and Rockwood trailers because excess slack in air conditioner wiring may contact heating elements, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0016-2017·2016-10-12

    Panoramic PC-1000 X-ray Systems Recalled for Safety Nut Defect

    Panoramic Rental Corp. is voluntarily correcting PC-1000 X-ray systems because a safety nut may be ineffective, posing a risk of blunt force trauma to the head, neck, or shoulders.

    Product
    Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V727000·2016-10-12

    Keystone Recalls 2017 Dutchmen Coleman Trailers for Wiring Fire Risk

    Keystone RV is recalling 84 model year 2017 Dutchmen Coleman recreational trailers because loose or frayed wiring in the power center may increase the risk of a fire.

    Product
    DUTCHMEN — DUTCHMEN COLEMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide