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.

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.

41501–41525 of 78321

  • SevereNHTSA·18V265000·2018-04-25

    Lakota Recalls 2018-2019 Trailers Due to Ramp Detachment Risk

    Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because missing hardware may allow the rear ramp to detach while moving, increasing crash risk.

    Product
    LAKOTA — LAKOTA BIGHORN, CHARGER, COLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1411-2018·2018-04-25

    Philips Brilliance Big Bore CT Systems Recalled for Emergency Stop Defect

    Philips is recalling 119 Brilliance Big Bore CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient load or unload.

    Product
    Brilliance Big Bore (Radiology) - Model no. 728244, 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 (Devices)·Z-1434-2018·2018-04-25

    Philips Panorama 1.0T MRI Recalled for Helium Gas Release Risk

    Philips is recalling Panorama 1.0T MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.

    Product
    Panorama 1.0T, Model 781250 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-1430-2018·2018-04-25

    Philips Multiva MRI Systems Recalled for Helium Gas Risk During Quench

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

    Product
    Multiva systems, 1) Multiva 1.5T 8 R5 Model 781072, 2) Multiva 1.5T 16 R5 Model 781073, 3) Multiva 1.5T 8ch R5 based Model 781074, 4) Multiva 1.5T Model 781076, & 5) Multiva 1.5T 16ch R5 based Model 781078 Product Usage: Indicated for use as a diagnostic device. It can…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1382-2018·2018-04-25

    Draeger Infinity Acute Care System Recall for Alarm Failure

    Draeger Medical Systems is recalling Infinity Acute Care System monitoring solutions because invasive pressure alarms may not activate.

    Product
    Infinity Acute Care System (IACS) Monitoring Solution, Catalog Numbers: MS18841, MS20401, MS20407, MS20724, MS22956, MS25510, MS25520, MS25643, MS26196, MS26372, MS31818; UDI Information: 4049098054454, 4049098054447, 4049098054409, 4049098009799, 4049098009751…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1379-2018·2018-04-25

    Getinge Washer-Disinfector Accessory Recall for Potential Cart Unloading Hazard

    Getinge is recalling 170 automated loading/unloading accessories for Washer-Disinfector 86 Series units due to a risk of disinfected goods falling to the floor.

    Product
    Getinge AGS, FSLC, FSUC, RC accessory to Washer- Disinfector 86 Series UDI Info: 86 Series Washer Disinfector 07340153700246, 07340153700253, 07340153700260, 07340153700277 Getinge automated loading/unloading systems are intended to be used as an automatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1140-2018·2018-04-25

    Funky Chunky Chocolate Pretzels Recalled for Undeclared Tree Nuts and Peanuts

    Funky Chunky LLC is recalling Chocolate Pretzels because they may contain undeclared tree nuts and peanuts. The recall covers 172 lbs of product distributed nationwide.

    Product
    funky chunky Chocolate Pretzels. Pretzels, Caramel, Chocolate, Pecans. Sold in the following packaging configurations: 1. Small Bag Net Wt. 2 oz. (56g) UPC 91056-00045; 2. Large Bag Net Wt. 5 oz. (141g) UPC 91056-00040; 3. Mini Canister Net Wt. 8 oz. (227g) UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1022-2018·2018-04-25

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

    Mrs. Gerry's is recalling specific lots of Kwik Trip Egg Salad because they may contain undeclared traces of imitation crab meat.

    Product
    Mrs. Gerry's Kwik Trip Egg Salad, Net Wt. 35 lb. (15.87kg), UPC 17839-61135. Keep Refrigerated. Manufactured by Mrs. Gerry's, Albert Lea, MN 56007
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1437-2018·2018-04-25

    Philips Ingenia 1.5T CX MRI Recall for Helium Gas Risk

    Philips is recalling Ingenia 1.5T CX MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.

    Product
    Ingenia 1.5T CX, Models 781261 & 781262 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-1023-2018·2018-04-25

    Mrs. Gerry's Egg and Potato Salads Recalled for Undeclared 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 Homestyle Egg Salad, Net Wt. 5 lb. (2.27kg), UPC 17839-60905. Keep Refrigerated. Manufactured by Mrs. Gerry's, Albert Lea, MN 56007
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1436-2018·2018-04-25

    Philips MRI Software Recall Due to Helium Gas Risk During Quench

    Philips is recalling the SmarthPath to dStream conversion software for 1.5T MRI systems due to a potential risk of helium gas release during a magnet quench.

    Product
    Conversion SmarthPath to dStream for 1.5T, Model 781260 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-1415-2018·2018-04-25

    Philips Brilliance 6 Slice CT System Recalled for Emergency Stop Defect

    Philips is recalling Brilliance 6 Slice CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading.

    Product
    Brilliance 6 Slice (Air) - Model no. 728256, 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 (Devices)·Z-1441-2018·2018-04-25

    Philips Multiva MRI Systems Recalled for Helium Gas Quench Risk

    Philips is recalling 8,205 Multiva MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.

    Product
    Multiva systems; 1) Magnets Multiva 16 Model 781487, 2) Magnets 8 Model 781488, 3) Magnet Achieva 1.5T, Model 781492, 4) Magnet HFO, Model 781495, 5) Magnet Multiva 16, Model 781496, 6) Magnet Multiva 8, Model 781497 & 7) Magnets Ingenia 1.5T CX, Model 781498 Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1432-2018·2018-04-25

    Philips Intera 1.0T MRI Systems Recalled for Helium Gas Risk

    Philips is recalling 8,205 Intera 1.0T MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.

    Product
    Intera 1.0T; 1) Stellar Model 781102, 2) Pular Model 781103 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-1405-2018·2018-04-25

    Philips Ingenuity CT Recall for Emergency Stop Defect

    Philips is recalling 172 Ingenuity CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient load or unload.

    Product
    Ingenuity CT - Model no. 728326, 728325, 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-1412-2018·2018-04-25

    Philips Brilliance 16 Slice CT System Recalled for Emergency Stop Defect

    Philips is recalling two Brilliance 16 Slice CT systems because the emergency stop may fail to disable the horizontal motor, allowing the couch to move during patient loading.

    Product
    Brilliance 16 Slice (Air) - Model no. 728246, 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-1032-2018·2018-04-25

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

    Mrs. Gerry's Market Fresh Potato Salad is being recalled because it may contain undeclared traces of imitation crab meat, a potential allergen.

    Product
    Mrs. Gerry's Market Fresh Potato Salad Net Wt. 12 lbs. (5.44 kg), UPC 17839-94212. Keep Refrigerated. Manufactured by Mrs. Gerry's, Albert Lea, MN 56007
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1425-2018·2018-04-25

    Carefusion Recalls Jamshidi Needles Due to Compromised Sterile Packaging

    Carefusion 2200 Inc is recalling 14,200 Jamshidi (TJ) needles because the integrity of the sterile packaging is potentially compromised.

    Product
    JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5, b.) 8G x 4, c.) 11G x 3.5, d.) 8G x 6, e.) 11G x 6]; STERILE;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1026-2018·2018-04-25

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

    Mrs. Gerry's Kitchen is recalling Original Potato Salad because it may contain undeclared traces of imitation crab meat, a potential allergen.

    Product
    Mrs. Gerry's Original Potato Salad, Packaged into the following size containers: 1. Net Wt. 1 lb. (454 g) UPC 17839-10201, 2. Net Wt. 13 lb. (5.89 kg), UPC 17839-10213. 3. Net Wt. 35 lb. (15.87 kg), UPC 17839-10235 Keep Refrigerated. Manufactured by Mrs. Gerry's…
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1374-2018·2018-04-25

    Tornier Recalls Phantom Fiber Sutures Due to Potential Strength Loss

    Tornier, Inc. is recalling 32,253 units of Phantom Fiber sutures because improper storage may cause the raw material to degrade, leading to a loss of suture strength.

    Product
    Fornier Phantom Fiber(TM) Sutures: Item Number Description SMB000425 4.5 MM PHANTOM FT BIOCOMPOSITE SUTURE ANCHOR WITH NEEDLES SMB000525 5.5 MM PHANTOM FT BIOCOMPOSITE SUTURE ANCHOR WITH NEEDLES SMP000425 4.5 MM PHANTOM FT PEEK SUTURE ANCHOR WITH NEEDLES SMP000525 5.5 MM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1427-2018·2018-04-25

    Halyard Closed Suction System Flex Connectors May Disconnect During Use

    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, Double Swivel Elbow (DSE). Used to aspirate liquids or semisolids from a patient's upper airway. Labeled as the following: a. HALYARD* 12FR DSE 21.3IN/54CM (WHITE); b. HALYARD* 12 FR TRACH CARE DSE ENDO; c. HALYARD* 12FR DSE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1028-2018·2018-04-25

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

    Mrs. Gerry's Kitchen is recalling specific potato salad products 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 Deli Fresh Potato Salad, Net Wt. 1 lb. (454 g) UPC 17839-93001, Net Wt. 3 lb. (1.36 kg), UPC 17839-93003. Net Wt. 5 lb. (2.26 kg), UPC 17839-93005. Net Wt. 12 lb. (5.44 kg), UPC…
    Category
    Food
    Distribution
    12 states