The Recall Desk

State

Nebraska product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29876–29900 of 78302

  • SevereFDA (Drugs)·D-1407-2020·2020-08-05

    Saniderm Hand Sanitizer Recalled for Undeclared Methanol Contamination

    UVT INC is recalling Saniderm Advanced Hand Sanitizer because it contains undeclared methanol. The product was distributed nationwide in the USA.

    Product
    Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by Eskbiochem SA de CV, Mexico Japon 50, Celaya, Gto., Mexico, 38010. UPC 8 60003 63391 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V459000·2020-08-05

    Kia Recalls 2019 Forte Vehicles Due to Axle Driveshaft Defect

    Kia is recalling 2019 Forte vehicles because the left front axle driveshaft may not have been heat-treated, which can cause it to break and increase crash risk.

    Product
    KIA — KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2725-2020·2020-08-05

    Medline Recalls ClearPro Trach T-Piece Closed Suction Catheters

    Medline is recalling 680 units of ClearPro Trach T-Piece Closed Suction Catheters because the catheter may come apart from the device assembly during use.

    Product
    ClearPro Trach T-Piece Closed Suction Catheter, Model DYNCPTP14T, 14 Fr 12.5 IN FOR TRACHEOSTOMY TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2708-2020·2020-08-05

    TTDEYE Black Starshine Colored Contact Lenses Recalled for Lack of FDA Clearance

    Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Black Starshine colored contact lenses because they were distributed without FDA clearance.

    Product
    TTDEYE (brand) Black Starshine, B16112100 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2726-2020·2020-08-05

    Teleflex Rusch Greenlite Laryngoscopes Recalled for Welded Joint Breakage

    Teleflex Medical Inc. is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall affects 75,320 units distributed nationwide.

    Product
    Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2712-2020·2020-08-05

    TTDEYE Radial Brown Colored Contact Lenses Recalled for Lack of FDA Clearance

    Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Radial Brown colored contact lenses because they were distributed without FDA clearance.

    Product
    TTDEYE (brand) Radial Brown, B16112109 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2707-2020·2020-08-05

    Medtronic StealthStation S7 System Recalled for Navigation Inaccuracy

    Medtronic is recalling two StealthStation S7 Systems with Polaris Spectra Cameras due to a manufacturing issue that may cause 6mm navigation inaccuracy when using specific trackers.

    Product
    StealthStation" S7 System with Polaris Spectra Camera part number PSU 9733437 - Product Usage: are intended as an aid for precisely locating anatomical structures in either open or percutaneous procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2730-2020·2020-08-05

    Teleflex Recalls Rusch Greenlite Laryngoscopes Due to Welded Joint Breakage

    Teleflex Medical Inc is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The devices are used for tracheal intubation.

    Product
    Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20160·2020-08-05

    WD-40 Recalls X-14 Mildew Stain Remover Due to Skin Irritation Risk

    WD-40 Company is recalling specific 16 and 32-ounce bottles of X-14 Mildew Stain Remover because pressure buildup may cause leaks and skin irritation.

    Product
    X-14® Mildew Stain Remover
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V458000·2020-08-05

    Thor Motor Coach Motorhomes Recalled: Pedestal Bolts May Fail During Crash

    Thor Motor Coach is recalling 2020-2021 Daybreak, 2018-2021 Four Winds, and 2018-2021 Chateau motorhomes because barrel chair pedestals are secured with bolts of the wrong size. In a crash, these pedestals could separate, causing seat belt anchorages to fail and increasing injury risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH redundant FOUR WINDS, redundant CHATEAU, DAYBREAK, FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2714-2020·2020-08-05

    TTDEYE Devil Red Colored Contact Lenses Recalled for Lack of FDA Clearance

    Chengdu Ai Qin E-commerce Co., Ltd. is recalling TTDEYE Devil Red colored contact lenses because they were distributed without FDA clearance.

    Product
    TTDEYE (brand) Devil Red, B16112201 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2728-2020·2020-08-05

    Teleflex Medical Recalls Rusch Greenlite Laryngoscopes Due to Welded Joint Breakage

    Teleflex Medical Inc. is recalling 7,401 Rusch Greenlite laryngoscopes because the welded joint may break during use.

    Product
    Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2731-2020·2020-08-05

    Teleflex Rusch Greenlite Laryngoscopes Recalled for Welded Joint Breakage

    Teleflex Medical is recalling Rusch Greenlite laryngoscopes because the welded joints may break. The devices are used for tracheal intubation.

    Product
    Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2724-2020·2020-08-05

    Medline Recalls ClearPro T-Piece Closed Suction Catheters Due to Assembly Failure

    Medline Industries is recalling 2,440 units of ClearPro T-Piece Closed Suction Catheters because reports indicate the catheter may come apart from the device assembly during use.

    Product
    ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2704-2020·2020-08-05

    United Imaging uCT 530 CT System Recalled for Sharp Metal Edge

    Shanghai United Imaging Healthcare is recalling four uCT 530 Computed Tomography X-ray Systems because uneven metal edge overlap may create a sharp edge.

    Product
    Computed Tomography X-ray System; Model uCT 530; Rx; UDI: (01) GTIN: 06971576831012 - Product Usage: intended to produce cross-sectional images of the body using computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2727-2020·2020-08-05

    Teleflex Recalls Rusch Greenlite Laryngoscopes Due to Welded Joint Breakage

    Teleflex Medical Inc is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall covers 27,341 units distributed nationwide.

    Product
    Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2705-2020·2020-08-05

    United Imaging uCT 550 CT Systems Recalled for Sharp Metal Edges

    Shanghai United Imaging Healthcare is recalling three uCT 550 Computed Tomography X-ray Systems because uneven metal edges on the mylar strip may create sharp edges.

    Product
    Computed Tomography X-ray System; Model uCT 550; Rx; UDI: (01) GTIN: 06971576831036 - Product Usage: intended to produce cross-sectional images of the body using computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2701-2020·2020-08-05

    Abbott Alinity ci System Control Module Recalled for Quality Control Failures

    Abbott is recalling Alinity ci System Control Modules because quality control results were not properly evaluated for failures.

    Product
    Alinity ci series System Control Module (SCM); LN 3R70-01 Alinity ci series software versions, 3.1.1 and below
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2703-2020·2020-08-05

    United Imaging uCT 760 CT Systems Recalled for Sharp Metal Edges

    Shanghai United Imaging Healthcare is recalling five uCT 760 CT systems because uneven metal edges on the mylar strip may create sharp edges.

    Product
    Computed Tomography X-ray System; Model uCT 760; Rx; UDI: (01) GTIN: 06971576831043 - Product Usage: intended to produce cross-sectional images of the body using computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2713-2020·2020-08-05

    TTDEYE Radial Pink Colored Contact Lenses Recalled for Lack of FDA Clearance

    Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Radial Pink colored contact lenses because they were distributed without FDA clearance.

    Product
    TTDEYE (brand) Radial Pink, B16112110 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2732-2020·2020-08-05

    Teleflex Medical Recalls Rusch Greenlite Laryngoscopes Due to Welded Joint Breakage

    Teleflex Medical Inc. is recalling 29,740 Rusch Greenlite laryngoscopes because the welded joint may break. The devices are used for tracheal intubation.

    Product
    Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2710-2020·2020-08-05

    TTDEYE Flower Brown Colored Contact Lenses Recalled for Lack of FDA Clearance

    Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Flower Brown colored contact lenses because they were distributed without FDA clearance.

    Product
    TTDEYE (brand) Flower Brown, B16112210 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1039-2020·2020-08-05

    Built Brands Recalls Peanut Butter Chocolate Protein Bars for Mold Risk

    Built Brands LLC is recalling 242,400 peanut butter chocolate protein bars because they may be moldy before the expiration date.

    Product
    Peanut Butter Chocolate covered protein bars, packaged in metalized polypropylene wrappers, packed in 6 count to 18 count boxes, net wt. ranges from 53 to 58 grams.
    Category
    Food
    Distribution
    Distributed nationwide