The Recall Desk

State

Nebraska product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58676–58700 of 78413

  • HighFDA (Devices)·Z-1326-2015·2015-04-01

    Ameda One-Hand Manual Breast Pump Recalled for Lack of Sterilization

    Ameda, Inc. is recalling 1,763 units of the One-Hand Manual Breast Pump (SKU 17161) because the devices were not sterilized.

    Product
    Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging is 6 pouches with Tyvek header (9.5 x 13.63 x 3.75") within a secondary corrugated shipper (16 x 11.02 x 5.12" inner dimensions). The device is indicated for assisted expression of milk using manual suction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1576-2015·2015-04-01

    Uncle Ben's Ready Rice Recalled for Potential Metal Fragments

    Mars Food US is recalling Uncle Ben's Ready Rice Butter & Garlic pouches due to the potential for containing metal fragments.

    Product
    UNCLE BEN'S(R) Ready Rice(R) BUTTER & GARLIC FLAVORED, Net Wt 8.8 oz (250 g),
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1305-2015·2015-04-01

    GE Healthcare Recalls MRI Systems Due to Software Maintenance Issues

    GE Healthcare is recalling 9,369 MRI systems worldwide because software versions were not maintained properly at some sites.

    Product
    GE Healthcare, SIGNA 1.5T TWINSPEED, SIGNA INFINITY MRISYSTEM, SIGNA 3.0T INFINITY WITH EXCITE, SIGNA 3.0T WITH EXCITE, SIGNA EXCITE 1.5T, SIGNA EXCITE 3.0T, GE 1.5T AND 3.0T SIGNA HDX MR SYSTEM, Discovery MR750 3.0T, Discovery MR450 1.5T, Discovery MR750w 3.0T, Optima MR450w…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1303-2015·2015-04-01

    Intuitive Surgical Recalls da Vinci Xi Systems Due to Sensor Fault

    Intuitive Surgical is recalling 167 da Vinci Xi Surgical Systems worldwide because a fault causes distal SUJ failures and position sensor mismatches.

    Product
    da Vinci Xi Surgical System, IS4000; ASSY,DISTAL SUJ,OUTER,IS4000, Material number: 380663-20 and 380663-21. The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1588-2015·2015-04-01

    Aloha Chocolate Premium Protein Powder Recalled for Staphylococcus Enterotoxin

    Aloha is recalling its Chocolate Premium Protein powder due to the presence of Staphylococcus enterotoxin. The product was sold nationwide online and in New York retail stores.

    Product
    ALOHA CHOCOLATE PREMIUM PROTEIN is a powder and , product is packed as the following: 1) Tin: UPC 641061842613, 2) Pouch: UPC 641061842651 and 3) Protein Tower 14 pack: UPC 640864820743. Formulated, Quality Tested & Exclusively Sold by ALOHA, Inc. NY, NY 10011 +1 888.444.3898
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1579-2015·2015-04-01

    Uncle Ben's Ready Rice Recalled for Potential Metal Fragments

    Mars Food US is recalling Uncle Ben's Ready Rice Original due to the potential presence of metal fragments.

    Product
    UNCLE BEN'S(R) Ready Rice(R) ORIGINAL, ENRICHED LONG GRAIN WHITE RICE, Net Wt 8.8 oz (250 g),
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1617-2015·2015-04-01

    FGF Brands Recalls Mini Naan for Missing Allergen and Nutrition Labels

    FGF Brands, Inc. is recalling 7,783 cases of Mini Naan because the packages were shipped without labels declaring ingredients, nutrition, or allergens.

    Product
    Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360 g) per package and old under the US Foods brand. Product is labeled with instructions to keep frozen until use. Eight (8) packages per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1302-2015·2015-04-01

    Intuitive Surgical Recalls da Vinci Xi Systems Due to Joint Sensor Fault

    Intuitive Surgical is recalling 167 da Vinci Xi Surgical Systems worldwide due to a fault causing distal sensor failures and position mismatches.

    Product
    da Vinci Xi Surgical System, IS4000; Assy, Distal SUJ, Inner, IS4000 Material number: 380662-20 and 380662-21. The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1575-2015·2015-04-01

    Uncle Ben's Ready Rice Recalled for Potential Metal Fragments

    Mars Food US is recalling Uncle Ben's Ready Rice Roasted Chicken Flavored with Carrots and Herbs due to the potential for containing metal fragments.

    Product
    UNCLE BEN'S(R) Ready Rice(R) ROASTED CHICKEN FLAVORED with Carrots and Herbs, Net Wt 8.8 oz (250 g),
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15E027000·2015-04-01

    Buy4easy Recalls TMS HY-809 Motorcycle Helmets for Impact Protection Defects

    Buy4easy is recalling TMS HY-809 motorcycle half-helmets because they may fail to adequately dampen impacts and lack required labeling, increasing injury risk in crashes.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1586-2015·2015-04-01

    Sunfood Recalls Organic Sacha Inchi Powder Due to Staphylococcus Enterotoxin Risk

    Sunfood is recalling Organic Sacha Inchi Powder because it may be contaminated with Staphylococcus enterotoxin. The product was distributed nationwide and internationally.

    Product
    Organic Sacha Inchi Powder, 8oz. white poly bags, UPC 803813-28444 1. Organic Sacha Inchi Powder, bulk.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1627-2015·2015-04-01

    Taj Ethnic Gourmet Calcutta Masala Simmer Sauce Recalled for Undeclared Peanut

    The Hain Celestial Group is recalling Taj Ethnic Gourmet Calcutta Masala Simmer Sauce because cumin in the product may contain undeclared peanut protein.

    Product
    Taj ETHNIC GOURMET CALCUTTA MASALA Simmer Sauce, NET WT 16.0 OZ. (454.0g), UPC 7 18687 30011 4
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1310-2015·2015-04-01

    RayStation Radiation Therapy Software Recalled for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation Radiation Therapy Treatment Planning System software due to an issue with photon dose calculation for Dynamic MLC plans.

    Product
    RayStation Radiation Therapy Treatment Planning System; -- RayStation 3.5, RayStation 4.0, RayStation 4.5 and RayStation 4.7. For RayStation 4.7, the issue applies also to machines with fixed jaws, regardless of MLC/jaw position. RayStation is a software system designed for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1306-2015·2015-04-01

    Penner Patient Stretcher/Transfer Lift System Recalled for Tipping Hazard

    Penner Mfg Inc is recalling 158 Patient Stretcher/Transfer Lift Systems because improper patient positioning could cause the device to tip, risking injury to patients or operators.

    Product
    Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift is used with Whirlpool or Aqua-Aire (air bubbling) bathing system intended for use in nursing homes, hospitals, and assisted living facilities to transfer and/or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1327-2015·2015-04-01

    Ameda Dual Short Term HygieniKit Milk Collections System Recalled for Lack of Sterilization

    Ameda is recalling its Dual Short Term HygieniKit Milk Collections System because the devices were not sterilized. Consumers should stop using the product and contact the manufacturer.

    Product
    Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115) - Primary packaging is 12 pouches with Tyvek header (10.75 x 16.375 x 3") within a secondary corrugated shipper (20.75 x 15.50 x 8.5" inner dimensions). The device is intended to be connected to a powered…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1304-2015·2015-04-01

    Intuitive Surgical Recalls da Vinci Xi Systems Due to Sensor Fault

    Intuitive Surgical is recalling 167 da Vinci Xi Surgical Systems worldwide due to a fault causing distal SUJ failures and position sensor mismatches.

    Product
    da Vinci Xi Surgical System, IS4000; ASSY,USM,IS4000, Material number: 380647-20 and 380647-22 The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive Surgical Endocopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1308-2015·2015-04-01

    Siemens MAGNETOM MRI Systems Recalled for Gradient Output Supervision Defect

    Siemens Medical Solutions is recalling 132 MAGNETOM MRI systems because a defect in gradient output supervision could allow outputs to exceed safety limits, potentially causing peripheral nerve stimulation.

    Product
    MAGNETOM systems Aera/Skyra/Avanto/Verio with software syngo MR D13A ; indicated for use as magnetic resonance diagnostic devices (MRDD) that produce transverse, sagittal, coronal and oblique cross-sectional images, spectroscopic images and/or spectra, and that display the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1577-2015·2015-04-01

    Uncle Ben's Ready Rice Recalled for Potential Metal Fragments

    Mars Food US is recalling Uncle Ben's Ready Rice New Orleans Style Red Beans & Rice due to the potential for containing metal fragments.

    Product
    UNCLE BEN'S(R) Ready Rice(R) NEW ORLEANS STYLE RED BEANS & RICE, with a blend of smokey, savory seasonings, Net Wt 8.5 oz (240 g),
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1628-2015·2015-04-01

    Taj Ethnic Gourmet Punjabi Saag Spinach Sauce Recalled for Undeclared Peanut

    The Hain Celestial Group is recalling Taj Ethnic Gourmet Punjabi Saag Spinach Sauce because it may contain undeclared peanut protein.

    Product
    Taj ETHNIC GOURMET PUNJAB SAAG Spinach Sauce, NET WT 16.0 OZ. (454.0g), UPC 7 18687 30013 8
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1311-2015·2015-04-01

    CareFusion Recalls Alaris PC Infusion Pumps Due to Keypad Error Code

    CareFusion 303, Inc. is recalling 56,015 Alaris PC infusion pumps because a keypad issue may trigger an error code during the power-on self-test.

    Product
    Alaris PC units, Model No. 8015. Infusion pump.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1313-2015·2015-04-01

    Synthes Electric Pen Drive Hand Switch Labeling Error Recall

    Synthes, Inc. is recalling 249 Electric Pen Drive systems because the Hand Switch labels for 'on' and 'lock' were interchanged.

    Product
    Synthes Electric Pen Drive (EPD) System, The Synthes Electric Pen Drive is indicated for screw insertion, pin and wire replacement, cutting of bone and metal, drilling, decorticating, shaping, and smoothing of bones and teeth in a wide variety of surgical procedures, including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0420-2015·2015-04-01

    West-Ward Recalls Fentanyl Citrate Injections Due to Impurity Failures

    West-Ward Pharmaceutical is recalling Fentanyl Citrate injections because the product failed impurity and degradation specifications and 12-month stability testing.

    Product
    FENTANYL CITRATE — FENTANYL CITRATE (FENTANYL CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1323-2015·2015-04-01

    ArthroCare Recalls 15 Coblator II Systems Due to Component Reversal

    ArthroCare Medical Corporation is recalling 15 Coblator II systems because specific components were reversed on the controller boards.

    Product
    Coblator II System, 120V. Product Usage: The Coblator II (Model RF8000E) is a bipolar, radiofrequency electrosurgical system designed for use in otorhinolaryngology (ENT) surgery. The system consists of the following components: an electrosurgical radiofrequency controller…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1321-2015·2015-04-01

    Siemens ADVIA Chemistry Systems Drug Calibrator I Recalled for Incorrect Values

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Systems Drug Calibrator I, lot 3JD018, due to incorrect calibrator values for Phenytoin 2 and Phenobarbital 2 assays.

    Product
    ADVIA Chemistry Systems Drug Calibrator I; For in vitro diagnostic use in the calibration of Phenobarbital_2 (PHNB_2), Phenytoin_2 (PHNY_2), and Theophylline_2 (THEO_2) methods on the ADVIA Chemistry systems. System Information: (For Information Only) The ADVIA Chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide