The Recall Desk

State

Nebraska product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41526–41550 of 78321

  • HighFDA (Food)·F-1025-2018·2018-04-25

    Mrs. Gerry's Deviled Egg Potato Salad Recalled for Undeclared Crab Meat

    Mrs. Gerry's Kitchen is recalling Deviled Egg Potato Salad because it may contain undeclared traces of imitation crab meat.

    Product
    Mrs. Gerry's Deviled Egg Potato Salad, Packaged into the following size containers: 1. Net Wt. 3 lb. (1.36 kg) UPC 17839-09003, 2. Net Wt. 5 lb. (2.26 kg), UPC 17839-09005. 3. Net Wt. 12 lb. (5.45 kg), UPC 17839-09012 Keep Refrigerated. Manufactured by Mrs.…
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1407-2018·2018-04-25

    Philips Ingenuity Core 128 CT Systems Recalled for Emergency Stop Defect

    Philips is recalling 591 Ingenuity Core 128 CT systems because closing the emergency stop may allow the patient couch to move during loading or unloading.

    Product
    Ingenuity Core 128 - Model no. 728323, 728324, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1029-2018·2018-04-25

    Potato and Egg Salads Recalled for Undeclared Imitation Crab Meat

    Mrs. Gerry's Kitchen is recalling various potato and egg salads because they may contain undeclared traces of imitation crab meat.

    Product
    Potato Salad packaged in the following branded and sized containers: 1. Mrs. Gerry's Old Fashioned Potato Salad, Net Wt. 1 lb. (454 g) UPC 17839-94101, Net Wt. 3 lb. (1.36 kg), UPC 17839-94103. Net Wt. 5 lb. (2.27 kg), UPC 17839-94105. Keep Refrigerated. Manufactured…
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1027-2018·2018-04-25

    Mrs. Gerry's Potato Salads Recalled for Undeclared Imitation Crab Meat

    Mrs. Gerry's is recalling various egg and potato salads because they may contain undeclared traces of imitation crab meat.

    Product
    Mrs. Gerry's Gourmet Potato Salad, Net Wt. 12 lb. (5.44 kg), UPC 17839-10112. Keep Refrigerated. Manufactured by Mrs. Gerry's, Albert Lea, MN 56007.
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1440-2018·2018-04-25

    Philips T10-NT MRI Systems Recalled for Helium Gas Risk

    Philips is recalling 8,205 T10-NT MRI systems due to a potential risk of helium gas release in the examination room during a magnet quench.

    Product
    T10-NT, Model 78107 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1399-2018·2018-04-25

    Siemens Oncor Expression Linear Accelerator Software Update Recall

    Siemens is recalling two Oncor Expression linear accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    ONCOR Expression, Digital Linear Accelerator, Model No. 07360717 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1429-2018·2018-04-25

    Halyard Closed Suction System Recall Due to Loose Flex Connectors

    Halyard Health is recalling certain Closed Suction Systems because the Flex Connectors may become loose or disconnect before or during use.

    Product
    Halyard Closed Suction System for Adults, Multi-Access¿Port¿Closed¿Suction¿System¿for¿Adults. Used to aspirate liquids or semisolids from a patient's upper airway. a. HALYARD* MULTI-PORT, DSY, ENDO 10FR; b. HALYARD* MULTI-PORT, DSY, ENDO 12FR; c. HALYARD* MULTI-PORT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1396-2018·2018-04-25

    Philips Brilliance 64 CT Scanner Software Defect Recall

    Philips is recalling 291 Brilliance 64 CT scanners because a software defect prevents Surview scans from initializing when tube current is below 30 mA.

    Product
    Brilliance 64 with 4.1.7 XX026 software version model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1404-2018·2018-04-25

    Philips Ingenuity Flex CT Scanner Recall for Emergency Stop Defect

    Philips is recalling 151 Ingenuity Flex CT scanners because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading.

    Product
    Ingenuity Flex - Model no. 728317, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1380-2018·2018-04-25

    Getinge Washer-Disinfector Accessory Recall Due to Unloading Hazard

    Getinge is recalling 170 automated loading/unloading systems for Washer-Disinfector 88 Series units. The recall addresses a risk that disinfected goods may fall to the floor if the trolley is not docked.

    Product
    Getinge AGS, FSLC, FSUC, RC accessory to Washer- Disinfector 88 Series UDI Info: 07340153700109, 07340153700116 Getinge automated loading/unloading systems are intended to be used as an automatic conveyor/transport system for unloading carriers (wash carts) from Getinge…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1398-2018·2018-04-25

    Siemens Oncor Avant-garde Linear Accelerator Software Update Recall

    Siemens is recalling one Oncor Avant-garde linear accelerator to update software and reduce the risk of collision during automated cancer treatments.

    Product
    ONCOR Avant-garde, Digital Linear Accelerator, Model No. 05863472 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1424-2018·2018-04-25

    Carefusion 2200 Recalls Jamshidi Bone Marrow Needles Due to Packaging Integrity

    Carefusion 2200 Inc is recalling sterile Jamshidi bone marrow needles because the integrity of the sterile packaging is potentially compromised.

    Product
    JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5, b.) 8G x 4, c.) 11G x 4, d.) 8G x 6, e.) 11G x 6]; STERILE;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1377-2018·2018-04-25

    Cook Inc. Recalls MINC Benchtop Incubators Due to Temperature Control Defect

    Cook Inc. is recalling 483 MINC Benchtop Incubators because a heater failure may cause temperatures to become too high or too low for proper cell culture.

    Product
    MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000 US) G46022 is a microprocessor controlled, gassed, humidified, incubator intended for use in cell culture.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1438-2018·2018-04-25

    Philips T5-NT MRI Scanner Recalled for Helium Gas Risk

    Philips is recalling 8,205 T5-NT MRI scanners worldwide due to a potential risk of helium gas release in the examination room during a magnet quench.

    Product
    T5-NT, Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1024-2018·2018-04-25

    Mrs. Gerry's Egg Salad Recalled for Undeclared Imitation Crab Meat

    Mrs. Gerry's Kitchen is recalling 5 lb. Egg Salad products because they may contain undeclared traces of imitation crab meat.

    Product
    Mrs. Gerry's Egg Salad, Net Wt. 5 lb. (2.26kg), UPC 17839-60605. Keep Refrigerated. Manufactured by Mrs. Gerry's, Albert Lea, MN 56007
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1413-2018·2018-04-25

    Philips Brilliance 64 CT System Recalled for Emergency Stop Defect

    Philips Medical Systems is recalling six Brilliance 64 CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.

    Product
    Brilliance 64 - Model no. 728231, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1433-2018·2018-04-25

    Philips Intera 1.5T MRI Systems Recalled for Helium Gas Risk

    Philips is recalling Intera 1.5T MRI systems due to a potential risk of helium gas release during a magnet quench.

    Product
    Intera 1.5T; 1) Intera 1.5T Omni/Stellar Model 781104, 2) Intera 1.5T Power/Pulsar Model 781105, 3) Intera 1.5T Master/Nova Model 781106, 4) Intera 1.5T Master CV Model 781107, 5) Intera 1.5T Explorer/ Nova Dual Model 781108, 6) Intera 1.5T IT Model 781160, 7) Intera 1.5T…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1378-2018·2018-04-25

    Cook Inc. Recalls MINC Benchtop Incubators Due to Temperature Control Defect

    Cook Inc. is recalling 4,451 MINC Benchtop Incubators because a heater defect may cause temperatures to become too high or too low for proper cell culture.

    Product
    MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a microprocessor controlled, gassed, humidified, incubator intended for use in cell culture.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1414-2018·2018-04-25

    Philips IQon Spectral CT Recalled for Emergency Stop Defect

    Philips is recalling 47 IQon Spectral CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.

    Product
    IQon Spectral CT - Model no. 728332, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1107-2018·2018-04-25

    Hungry Jack Pancake and Waffle Mix Recalled for Salmonella

    The J.M. Smucker Company is recalling Hungry Jack Original Pancake & Waffle Mix because the product tested positive for salmonella.

    Product
    HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-1401-2018·2018-04-25

    Siemens Oncor Impression Plus Linear Accelerator Software Recall

    Siemens is recalling 15 Oncor Impression Plus linear accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    ONCOR Impression Plus, Digital Linear Accelerator, Model No. 05857912 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1389-2018·2018-04-25

    Stryker Power-LOAD Cot Fastening System Recalled for Broken Floor Plates

    Stryker is recalling 4,724 Power-LOAD Cot Fastening Systems because the floor plates holding ambulance cot anchors may be broken.

    Product
    Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to assist with loading and unloading of a compatible wheeled stretcher (ambulance cot) to and from a transport vehicle and to secure the ambulance cot during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1410-2018·2018-04-25

    Philips CT Scanner Recall Due to Emergency Stop Defect

    Philips is recalling 106 Brilliance Big Bore CT scanners because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading or unloading.

    Product
    Brilliance Big Bore (Oncology) - Model no. 728243, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1030-2018·2018-04-25

    Festival Foods Potato Salad Recalled for Undeclared Imitation Crab Meat

    Mrs Gerry's Kitchen is recalling Festival Foods Potato Salad because it may contain undeclared traces of imitation crab meat.

    Product
    Festival Foods Potato Salad packaged in the following size containers: Net Wt. 6 oz. (170g), UPC 17839-22388, Net Wt. 1 lb. (454 g) UPC 17839-22301, Net Wt. 3 lb. (1.36 kg), UPC 17839-22303. Net Wt. 35 lb. 15.87 kg), UPC 17839-22335. Keep Refrigerated. Made for…
    Category
    Food
    Distribution
    12 states