The Recall Desk

State

Nebraska product recalls

72,907 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.

Which agencies issued them

These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1501–1525 of 77454

  • HighFDA (Devices)·Z-2288-2026·2026-06-10

    Philips Azurion 7B12 Roadmap Pro may produce unusable dark images

    Philips Azurion 7B12/12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0958-2026·2026-06-10

    Albertsons colossal Dubai cheesecake slice does not declare pistachio

    Albertsons store-made Cheesecake Slice Colossal Dubai is being recalled because the contains statement does not declare pistachio. 32 units are affected.

    Product
    UPC 25216200000 Cheesecake Slice Colossal Dubai. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2306-2026·2026-06-10

    GE MAC 5 ECG systems may link data to the wrong patient

    GE MAC 5 A4 and A5 Resting ECG Analysis Systems are being recalled because a development software version was released that can associate clinical information with the wrong patient.

    Product
    MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2309-2026·2026-06-10

    Sharpoint microsurgical knives labeled 2.2mm actually measure 3.0mm

    Sharpoint 2.2 mm angled double-bevel microsurgical knives are being recalled because 3.0 mm knives were labeled and packaged as 2.2 mm. 1,818 units affected.

    Product
    Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2279-2026·2026-06-10

    CASE cardiac testing systems may spark at the printer head

    CASE v7.0 Cardiac Testing Systems are being recalled because electrical sparking may occur at the printer head, and ignition of thermal paper could cause serious thermal injury.

    Product
    CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0554-2026·2026-06-10

    Spectra lidocaine ampules recalled over lack of sterility assurance

    Lidocaine HCl Injection USP in 5 mL single-dose ampules distributed by Spectra Medical Devices is being recalled for lack of assurance of sterility. 210,625 ampules affected.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE ANHYDROUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0959-2026·2026-06-10

    Albertsons catering loaf cake platter does not declare walnut

    Albertsons store-made Platter Catering Loaf Cake Slice is being recalled because the contains statement does not declare walnut. 92 units are affected.

    Product
    UPC 22418000000 Platter Catering Loaf Cake Slice. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·26V381000·2026-06-10

    Denago EV Recalls Multiple Models for Missing Pedestrian Warning Sounds

    Denago EV is recalling 2024-2026 electric vehicles that may fail to emit pedestrian warning sounds, increasing the risk of crashes.

    Product
    DENAGO EV — DENAGO EV NOMAD XL, ROVER XL, ROVER XL6, ROVER XXL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2307-2026·2026-06-10

    Aligned Medical fluids kits contain recalled lidocaine injection

    Aligned Medical AMS16835 Fluids Kits are being recalled because they include Lidocaine Hydrochloride Injection, USP that was recalled by a supplier for quality issues.

    Product
    Aligned Medical AMS16835 Fluids Kit RX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2291-2026·2026-06-10

    Philips Azurion 7M20 Roadmap Pro may produce unusable dark images

    Philips Azurion 7M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0981-2026·2026-06-10

    Cream cheese filled banana nut muffins do not declare walnut

    Albertsons store-made Muffins Banana Nut Cream Cheese Filled 2 count are being recalled because the contains statement does not declare walnut. Nine units are affected.

    Product
    UPC 25312600000 MUFFINS BANANA NUT CREAM CHEESE FILLED 2CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1023-2026·2026-06-10

    Pad Thai chicken ready meals do not declare anchovy

    Albertsons store-made Wok Pad Thai Chicken ready meals are being recalled because the contains statement does not declare anchovy.

    Product
    UPC 21208300000 Ready Meals WOK PAD THAI CHICKEN SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1034-2026·2026-06-10

    Albertsons peanut butter chocolate chip bars do not declare almond

    Albertsons store-made Peanut Butter Chocolate Chip Bar with Pretzel is being recalled because the contains statement does not declare almond. 128 units are affected.

    Product
    UPC 24144500000 Ready Meals PEANUT BUTTER CHOCOLATE CHIP BAR With PRETZEL This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0577-2026·2026-06-10

    Equaline ultra strength antacid tablets contain small metallic particles

    Equaline Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    EQU ULTRA STRENGTH ANTACID ASSORTED FRUIT 171AF — EQU ULTRA STRENGTH ANTACID ASSORTED FRUIT 171AF (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1029-2026·2026-06-10

    Albertsons sliced loaf platter does not declare walnut allergen

    Albertsons store-made Platter Loaf Sliced, 20 count, is being recalled because the contains statement does not declare walnut. 20 units are affected.

    Product
    UPC 22650200000 PLATTER LOAF SLC 20CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2299-2026·2026-06-10

    BD Pyxis Anesthesia Station fingerprint scanner may overheat and burn

    The BD Pyxis Anesthesia Station ES is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 4,579 units affected.

    Product
    BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0970-2026·2026-06-10

    Albertsons Mexican wedding cookies do not declare pecan allergen

    Albertsons store-made Mexican Wedding Cookies, 8 count, are being recalled because the contains statement does not declare pecan. 445 units are affected.

    Product
    UPC 22358600000 COOKIES MEXICAN WEDDING 8 CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1026-2026·2026-06-10

    Albertsons Cheeses of France platter does not declare almond

    Albertsons store-made Platter Cheeses of France is being recalled because the contains statement does not declare almond. 31 units are affected.

    Product
    UPC 27837800000 PLATTER CHEESES OF FRANCE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0962-2026·2026-06-10

    Chocolate lady madeleine strawberry cakes do not declare almond allergen

    Albertsons store-made Cake Pav Chocolate Lady Madeleines Strawberry is being recalled because the contains statement does not declare almond. Six units are affected.

    Product
    UPC 25491700000 Cake Pav Chocolate Lady Madeleines Strawberry. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0968-2026·2026-06-10

    Albertsons gourmet Dubai cookies do not declare pistachio

    Albertsons store-made Gourmet Dubai Cookie is being recalled because the contains statement does not declare pistachio.

    Product
    UPC 25185700000 COOKIE GOURMET DUBAI 1CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2302-2026·2026-06-10

    BD Pyxis MedStation fingerprint scanners may overheat and cause burns

    BD Pyxis MedStation ES Tower medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2301-2026·2026-06-10

    BD Pyxis Mini Main cabinets may overheat at fingerprint scanner

    BD Pyxis Mini Main medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 709 units affected.

    Product
    BD Pyxis Mini Main REF: 349 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0983-2026·2026-06-10

    Albertsons sticky bran muffins do not declare walnut allergen

    Albertsons store-made Sticky Bran Muffins, 4 count, are being recalled because the contains statement does not declare walnut. 105 units are affected.

    Product
    UPC 25524000000 MUFFINS STICKY BRAN 4CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2290-2026·2026-06-10

    Philips Azurion 7M12 Roadmap Pro may produce unusable dark images

    Philips Azurion 7M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide