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.

37451–37475 of 78321

  • SevereFDA (Drugs)·D-0986-2019·2019-03-13

    Sunstone Organics Recalls Maeng Da Kratom Powder Due to Salmonella Contamination

    Sunstone Organics is recalling Maeng Da Kratom powder in 25, 50, and 100-gram packages due to positive Salmonella test results.

    Product
    Maeng Da Kratom, packaged in a) 25 gram powder (UPC 00859667007118), b) 50 gram powder (UPC 00859667007125), c) 100 gram powder (UPC 00859667007132), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1171-2019·2019-03-13

    Kingston Pharma Recalls DG Baby Gripe Water Due to Undissolved Ingredient

    Kingston Pharma LLC is recalling DG Baby Gripe Water herbal supplements because they contain an undissolved ingredient, citrus flavonoid.

    Product
    DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary Supplement UPC: 8 54954 00246 3
    Category
    Food
    Distribution
    43 states
  • SevereFDA (Drugs)·D-0987-2019·2019-03-13

    Sunstone Organics Recalls White Vein Kratom Powder Due to Salmonella

    Sunstone Organics is recalling White Vein Kratom powder in 25, 50, and 100-gram packages because samples tested positive for Salmonella.

    Product
    White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder (UPC 00859667007323), c) 100 gram powder (UPC 00859667007330), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·19V197000·2019-03-13

    Newmar Recalls 2017-2019 Ventana Motorhomes for Loose Steering Bolts

    Newmar is recalling 2017-2019 Ventana motorhomes because loose steering and tie rod arm bolts may separate, causing loss of vehicle control and increasing crash risk.

    Product
    NEWMAR — NEWMAR VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0865-2019·2019-03-13

    Raindrop Near Vision Inlay Recalled Due to Increased Risk of Corneal Haze

    RVO 2.0, Inc. is recalling Raindrop Near Vision Inlays because a post-approval study found an increased risk of corneal haze following implantation.

    Product
    Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Devices)·Z-0975-2019·2019-03-13

    Draegar Medical Systems Recalls Omega Patient Monitor Software

    Draegar Medical Systems is recalling Omega patient monitor software due to cybersecurity vulnerabilities that may cause device reboots or loss of functionality.

    Product
    Omega Systems These devices are intended to be used in the environment where patient care is provided by Healthcare Professionals, i.e. Physicians, Nurses, and Technicians, who will determine when use of the device is indicated, based upon their professional assessment of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0985-2019·2019-03-13

    Siemens Uroskop Omnia Max Fluoroscopic X-ray System Recall for Swivel Arm Defect

    Siemens is recalling 191 Uroskop Omnia Max fluoroscopic X-ray systems because the swivel arm holding the monitors may become dislodged from the carrying arm.

    Product
    Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0984-2019·2019-03-13

    Siemens Uroskop Omnia Fluoroscopic X-ray System Recalled for Monitor Arm Defect

    Siemens is recalling six Uroskop Omnia fluoroscopic X-ray systems because the swivel arm holding the monitors may become dislodged from the carrying arm.

    Product
    Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop Omnia is a solid state detector fluoroscopic X-ray system, primarily for urological applications (functional x-ray diagnosis, endourology and minimal invasive urology/surgery).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0973-2019·2019-03-13

    Stryker Reprocessed Arthroscopic Shavers Recalled for Display and Function Errors

    Stryker is recalling 14,265 reprocessed arthroscopic shavers that may display incorrect settings or error messages, preventing proper use during surgery.

    Product
    Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut and excise tissue and bone; remove loose fragments; and, shave away debris in arthroscopic surgeries, as well as surgeries of the jaw and sinuses. Intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1143-2019·2019-03-13

    Meijer Recalls Chocolate Mint Chip Cookies Due to Undeclared Soy

    Meijer is recalling specific lots of Ultimate Chocolate Mint Chip Cookies because they contain undeclared soy. The recall covers products sold in Meijer stores nationwide.

    Product
    Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic clamshell 12 count UPC 4125014563 20 count UPC 4125014564
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V198000·2019-03-13

    TCI Recalls 2015 and 2017 Transtech Buses with Wheelchair Lift Defect

    Transportation Collaborative is recalling 2015 and 2017 Transtech buses because a wheelchair lift cam may fail, allowing the platform to rise too high and increase injury risk.

    Product
    TRANS TECH — TRANS TECH CST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0971-2019·2019-03-13

    Abbott Recalls Architect Magnesium Assay Due to Depressed Urine Results

    Abbott is recalling Architect Magnesium assays because urine tests may show falsely low results. The recall covers 24,995 units distributed in the US and four other countries.

    Product
    ARCHITECT MAGNESIUM, (a) REF 7D70-21, (b) 7D70-31 The Magnesium assay is used for the quantitation of magnesium in human serum, plasma, or urine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0974-2019·2019-03-13

    Draeger Infinity Delta Patient Monitors Recalled for Cybersecurity Vulnerabilities

    Draeger Medical Systems is recalling Infinity Delta patient monitors due to cybersecurity vulnerabilities that may cause device reboots or loss of functionality.

    Product
    Infinity Delta Family patient monitors The Infinity Delta Series (Delta/Delta XL/Kappa) monitors are intended to be used on adult, pediatric, and neonatal populations, with the exception of the parameter Cardiac Output, ST Segment Analysis, and arrhythmia which are intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19080·2019-03-13

    H-E-B Recalls Sauté Pans Due to Glass Lid Laceration Hazard

    H-E-B is recalling Kitchen & Table 5.5 qt. Sauté Pans because the glass lids can crack or shatter, posing a laceration hazard.

    Product
    Kitchen & Table 5.5 qt. Sauté Pan with glass lid
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0970-2019·2019-03-13

    Pentax C2 CryoBalloon Controller Recalled for Overpressure Detection Failure

    Pentax of America Inc is recalling 45 C2 CryoBalloon Controllers because the device fails to detect balloon overpressure during specific nitrous oxide applications, posing a risk of patient injury.

    Product
    C2 CryoBalloon Controller, REF: FG-1017, with Controller Software v1.18.258 The C2 CryoBalloon Ablation System is intended to be used as a cryosurgical tool in the field of general surgery, specifically for endoscopic application and the ablation of dysplastic Barrett s…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1145-2019·2019-03-13

    Concord Foods Recalls Salsa Seasoning Mix for Undeclared Milk Allergen

    Concord Foods is recalling Mild Salsa Seasoning Mix packets because they contain undeclared milk, a major food allergen.

    Product
    Concord Fresh Success Mild Salsa Seasoning Mix, Packaged in a NET WT 1.05 OZ (30g) packet, UPC: 0 4140900229 5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0983-2019·2019-03-13

    Maquet Cardiovascular Recalls AXIUS Blower Mister Due to CO2 Flow Issues

    Maquet Cardiovascular is recalling AXIUS Blower Mister devices because a potential lack of carbon dioxide flow may cause procedural delays during off-pump coronary artery bypass surgery.

    Product
    AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is intended to clear an anastomotic site for improved visibility
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0981-2019·2019-03-13

    BD MAX Enteric Bacterial Panel Recalled for False Negative Results

    Becton Dickinson is recalling 1,583 BD MAX Enteric Bacterial Panel kits due to false negative results for specific bacterial targets.

    Product
    BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX Enteric Bacterial Panel performed on the BD MAX System is an automated in vitro diagnostic test for the direct qualitative detection and differentiation of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1066-2019·2019-03-13

    Ascend Recalls Tamsulosin Hydrochloride Capsules Due to Dissolution Failure

    Ascend Laboratories is recalling 3,072 bottles of Tamsulosin Hydrochloride 0.4 mg capsules because stability testing revealed high out-of-specification dissolution results.

    Product
    TAMSULOSIN HYDROCHLORIDE — TAMSULOSIN HYDROCHLORIDE (TAMSULOSIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1147-2019·2019-03-13

    Good Neighbor Pharmacy Vitamin D Supplement Recalled for Mislabeling

    Twenty-First Century Healthcare is recalling Good Neighbor Pharmacy Vitamin D 2000 IU tablets because they are mislabeled and may contain Co Q10.

    Product
    Good Neighbor Pharmacy, D 2000 IU, Dietary Supplement, UPC: 0-87701-40751-2, 30 tablets.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0982-2019·2019-03-13

    Cepheid Respiratory Control Panel Recalled for Reduced Expiration Date

    Microbiologics Inc is recalling Cepheid Respiratory Control Panels because the expiration date was reduced from 24 months to 13 months.

    Product
    Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1146-2019·2019-03-13

    Good Neighbor Pharmacy Co Q10 Capsules Recalled for Mislabeling

    Twenty-First Century Healthcare is recalling Good Neighbor Pharmacy Co Q10 200mg capsules because they are mislabeled and may contain Vitamin D.

    Product
    Good Neighbor Pharmacy, Co Q10 200mg Capsule, Dietary Supplement, UPC: 0-87701-40817-5, 30 capsules.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1142-2019·2019-03-13

    WTRMLN WTR Cold Pressed Watermelon Juice Recalled for Plastic Contamination

    World Waters is recalling 277,230 units of WTRMLN WTR Cold Pressed Watermelon Juice due to potential soft plastic contamination.

    Product
    Watermelon, WTRMLNWTR Cold Pressured, 12fl oz, Watermelon Flavor, Refrigerated
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0992-2019·2019-03-13

    Apotex Recalls Out-of-Sequence Contraceptive Tablets

    Apotex Inc. is recalling specific lots of Drospirenone and Ethinyl Estradiol tablets because they may be missing or placed incorrectly in the blister pack.

    Product
    Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.03 mg, 28 Tablets Blister, 1 Unit (NDC 60505-4183-1) packaged as 84 Tablets Blister, 3x1 Unit per carton (NDC 60505-4183-3), Rx Only, Manufactured for: Apotex Corp., Weston, FL 33326; Manufactured by: Oman Pharmaceutical…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0994-2019·2019-03-13

    Petra Hygienic Systems Recalls Athleticare Hand Soap Due to Triclosan

    Petra Hygienic Systems is recalling Athleticare Anti-Bacterial Hand Soap because it contains triclosan, an ingredient no longer permitted in over-the-counter antiseptic wash products.

    Product
    ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan), 0.25%, 4 litres/1.1 US Gallon bottles, packaged in 4 x 4 Litres/1.1 US gallons per case, Petra Hygienic Systems, Concord, ON L4K 4RS/ Reno, NV 89511, NDC 42326-550-01, UPC 0 65936 10335 5.
    Category
    Drug
    Distribution
    Distributed nationwide