The Recall Desk

State

Nebraska product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4851–4875 of 77487

  • CriticalFDA (Food)·H-0059-2026·2025-10-22

    Cut cantaloupe chunks recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling Cut Fresh Cantaloupe Chunks in several container sizes under the Fresh & Finest and Harvest Cuts brands for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Cantaloupe Chunks packaged into the following size containers some under brand names Fresh & Finest or Harvest Cuts: 1. CANTALOUPE CHUNKS "PRMK" 30/2 OZ 2. CANTALOUPE CHUNKS "HC" 6/6 OZ. Harvest Cuts UPC 7 90629-11820 9. 3. CANTALOUPE CHUNKS "HC" 24/8 OZ.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0061-2026·2025-10-22

    Cut fruit trays with strawberries recalled over potential Listeria contamination

    Wholesale Produce Supply is recalling Harvest Cuts 2.5 lb Cut Fresh Fruit Trays with Strawberries for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Fruit Tray with Strawberries. 2.5 LB Harvest Cuts. Keep Refrigerated. UPC 7 90629-08132 9. Packed by WPS, Minneapolois, MN
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-0067-2026·2025-10-22

    BF-XT40 bronchofiberscopes recalled for updated therapy equipment use instructions

    Olympus is recalling OES Bronchofiberscope BF Type XT40 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0068-2026·2025-10-22

    Cut fresh fruit mix recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling cut fresh fruit mix under several brands and sizes for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, Pineapple, and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix CHPG (MCT) 1/5 lb. 2. Fruit Medley "HC" 24/8 oz. Harvest Cuts UPC 7 90629-08008 7. 3. Fruit Mix CHPG (PAIL)
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0065-2026·2025-10-22

    Cut melon mix recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling cut fresh melon mix under several brands and sizes for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Melon Mix. Contains: Cantaloupe, Honeydew, Watermelon. Keep Refrigerated. Packed under the following brands and sizes: 1. Melon Mix "HC" 4/16 oz. Harvest Cuts UPC 7 90629-11844 5. 2. Melon Mix CHW (MCT) 1/5 lb. UPC 7 90629-11173 6. 3. Melon Mix Bowl "HC"
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-0057-2026·2025-10-22

    BF-P190 bronchovideoscopes recalled for clarified laser and coagulation instructions

    Olympus is recalling EVIS EXERA III Bronchovideoscope BF-P190 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0067-2026·2025-10-22

    Cantaloupe honeydew grape mix recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling cut fresh fruit mix of cantaloupe, honeydew and red grapes under several brands for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix "HC" 6/6oz. UPC 7 90629-11821 6. 2. Fruit Medley "F&F" 4/12 oz. Fresh & Finest UPC 0 70253-00573 2 3. Fruit Mix 4/16 oz,
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-0061-2026·2025-10-22

    BF-Q180 bronchovideoscopes recalled for updated laser and coagulation instructions

    Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type Q180 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V719000·2025-10-22

    Isuzu and Chevrolet axle stabilizer bracket bolts can crack and break

    Isuzu is recalling certain 2018-2026 Isuzu FVR and FTR and Chevrolet 6500XD and 7500XD vehicles because the axle stabilizer bracket bolts may crack and break, letting the bracket detach.

    Product
    CHEVROLET — CHEVROLET, ISUZU 6500XD, 7500XD, FTR, FVR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0038-2026·2025-10-22

    Canned fruit cocktail recalled over potential lead contamination in one lot

    Pacific Coast Producers is recalling 609 cases of canned fruit cocktail in 100% juice for potential contamination with lead.

    Product
    Fruit Cocktail IN 100% JUICE WITH ADDED INGREDIENTS; NET WT 15 OZ (425 g); Ingredients: Diced Peaches, Diced Pears, Water, Grapes, Peach Pulp and Juice, Pineapple Sectors, Pear Juice Concentrate, Halved Cherries (colored red with Carmine), Ascorbic Acid (to protect color).; Distr
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-0139-2026·2025-10-22

    TENACIO pumps without InhibiZone recalled over inflation and deflation issues

    Boston Scientific is recalling TENACIO Pump without InhibiZone, UPN 72404420, because of the potential for inflation or deflation performance issues or difficulties.

    Product
    TENACIO Pump without InhibiZone; UPN: 72404420;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0156-2026·2025-10-22

    LOGIQ P10 HD systems recalled over inaccurate liver steatosis measurement values

    GE is recalling 31 LOGIQ P10 R4.5 HD ultrasound systems running software R4.5.7 because the Ultrasound-Guided Attenuation Parameter measurement may display inaccurate liver steatosis values.

    Product
    LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0203-2026·2025-10-22

    Paclitaxel infusion sets recalled from one lot because IV sets may leak

    Baxter is recalling 27,072 CLEARLINK System Paclitaxel Sets from one lot because the IV sets may leak.

    Product
    CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activated Valve, 0.2 Micron Filter, CLEARLINK Luer Activated Valve, 10 drops/mL, 107-inch (2.7 meters), Product Code 2R8858
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0198-2026·2025-10-22

    Fourteen inch extension sets recalled from one lot because sets may leak

    Baxter is recalling 2,304 CLEARLINK System straight-type extension sets with a retractable collar from one lot because the IV sets may leak.

    Product
    CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 14-inch (35 centimeters), Product Code 2C8632
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0169-2026·2025-10-22

    Monitor display cables recalled over inadequate shielding and electromagnetic interference

    Spacelabs Healthcare is recalling 16,898 DVI display cables because inadequate shielding may allow electromagnetic interference with other electronically sensitive medical devices in use.

    Product
    Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0893-01 Software Version: N/A Product Description: 16 inch DVI-I to DVI-I male/male display cable. Component: Yes, the cable is an external display cable used with
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0022-2026·2025-10-22

    Sunscreen lotion recalled after failing total aerobic microbial count testing

    SV Labs Prescott is recalling 11,386 tubes of Aloe Up Sport Performance Sunscreen Lotion SPF 30 after the firm released and distributed product that failed total aerobic microbial count testing.

    Product
    Aloe Up Sport Performance Sunscreen Lotion SPF 30, 1 FL OZ (30 mL) per tube, Mfd. for: ALOE UP, 9700 W. 76th St., Ste 112, Eden Prairie, Minnesota 55344
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0187-2026·2025-10-22

    Dilation and curettage packs recalled after being sterilized more than once

    American Contract Systems is recalling D and C convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.

    Product
    Medical convenience kits IHDC30R D AND C PACK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0182-2026·2025-10-22

    Radiology procedure packs recalled after being sterilized more than once

    American Contract Systems is recalling radiology convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.

    Product
    Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0197-2026·2025-10-22

    Forty four inch extension sets recalled because the IV sets may leak

    Baxter is recalling 15,552 CLEARLINK System 44-inch straight-type extension sets from one lot because the IV sets may leak.

    Product
    CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 44-inch (111 centimeters), Product code 2C8610
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0168-2026·2025-10-22

    Twelve foot display cables recalled over inadequate shielding and interference

    Spacelabs Healthcare is recalling 820 twelve-foot DVI display cables because inadequate shielding may allow electromagnetic interference with other electronically sensitive medical devices in use.

    Product
    Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-12 Software Version: N/A Product Description: 12 foot DVI-I to DVI-I male/male display cable. Component: Yes, the cable is an external display cable used with
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0145-2026·2025-10-22

    Shoulder surgical planning software recalled over possible implant malalignment risk

    Kico Knee Innovation Company is recalling 21 ARVIS Shoulder systems after a complaint identified an issue with the AI surgical planning software that may cause implant malalignment.

    Product
    Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software Software Version: V2025.1.2 Product Description: Intended Use: The ARVIS" system is a computer-controlled navigation system intended to provide intra-operative mea
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0132-2026·2025-10-22

    Omnipod 5 app recalled because magnifying a field duplicates typed digits

    Insulet is recalling 174,013 units of the Omnipod 5 iOS app because using the iPhone magnifier on a manual entry field while typing can duplicate a digit.

    Product
    The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature of the iPhone, while simultaneously selecting a single number on the keyboard.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0131-2026·2025-10-22

    Carotid stent systems recalled because integrated filter may not fully open

    Contego Medical is recalling 568 Neuroguard IEP carotid stent systems because the integrated filter may not open, or may not fully open, during sheath retraction and filter knob operation.

    Product
    Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP System), REF: NG-0740-140-2, NG-NV-7-40, NG-0640-140-2, NG-NV-6-40
    Category
    Medical Device
    Distribution
    Distributed nationwide