The Recall Desk

State

Nebraska product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42626–42650 of 78386

  • SevereFDA (Drugs)·D-0322-2018·2018-02-14

    FDA Recalls Sterile Morphine Sulfate Preparations Due to Sterility Concerns

    Intrathecal Compounding Specialist, LLC is recalling sterile morphine sulfate preparations compounded between October 16 and November 17, 2017, due to a lack of sterility assurance.

    Product
    All sterile drug preparations remaining within expiry prepared from Morphine Sulfate PF Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0328-2018·2018-02-14

    Flawless Beauty Recalls Unapproved Glutathione Injectable Products Nationwide

    Flawless Beauty LLC is voluntarily recalling all lots of Tationil Glutathione and other products sold in kits. The recall is due to misbranding and the sale of unapproved new drugs under a court order.

    Product
    Tationil Glutathione, 600 mg/ 4 mL, polvere e solvente per soluzione iniettabile, Teofarma, s.r.l.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0321-2018·2018-02-14

    FDA Recalls Hydromorphone Sterile Drug Preparations for Lack of Sterility Assurance

    Intrathecal Compounding Specialist is recalling sterile drug preparations made from Hydromorphone Base Solution due to a lack of sterility assurance.

    Product
    All sterile drug preparations remaining within expiry prepared from Hydromorphone Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0332-2018·2018-02-14

    Flawless Beauty Recalls Sterilized Water for Injections Due to Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of sterilized water for injections sold in the U.S. because the products were marketed without FDA approval.

    Product
    Sterilized water for injections BP, 50 x 5 mL plastic ampules, Manufactured in India
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0557-2018·2018-02-14

    Recall of Covidien Emprint Percutaneous Antenna Due to Tip Disengagement

    FDA Class II recall of Covidien Emprint Percutaneous Antennas because the ceramic trocar tip may disengage from the needle shaft and remain in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 15cm (reinforced), Material CA15L2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0789-2018·2018-02-14

    Hiland Orange Juice Recalled for Undeclared Milk Allergen

    Hiland Dairy Foods Company LLC is recalling 522 one-gallon containers of Hiland Orange Juice because milk was detected in the product, but milk is not declared on the label.

    Product
    Hiland Orange Juice, 1 GAL (3.78 L) Hiland Dairy, Springfield, MO.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0554-2018·2018-02-14

    Mindray TD60 Transmitter Battery Charger Recalled for Overcharging Risk

    Mindray is recalling 203 TD60 Transmitter battery chargers used with the BeneVision Central Station because a damaged circuit board can cause the battery to overcharge and the case to swell.

    Product
    TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00
    Category
    Medical Device
    Distribution
    27 states
  • SevereFDA (Drugs)·D-0335-2018·2018-02-14

    Flawless Beauty Recalls Unapproved Glutathione Whitening Injection Kits

    Flawless Beauty LLC is voluntarily recalling all lots of TAD Glutathione Whitening Kits because the products were marketed without FDA approval.

    Product
    TAD Glutathione Whitening Kits lyophilized powder for injection, 600 mg vials, 10 vials + 10 amps x 4 mL, Manufactured by: Biomedica Foscama Industria, Ferentino, Italy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0333-2018·2018-02-14

    Flawless Beauty LLC Recalls Ling Zhi Capsules for Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of Ling Zhi capsules because they were marketed without an approved NDA/ANDA, constituting misbranding and unapproved new drugs.

    Product
    Ling Zhi capsules
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0323-2018·2018-02-14

    FDA Recalls Sufentanil Citrate Preparations Due to Sterility Concerns

    The FDA is recalling sterile drug preparations made from Sufentanil Citrate Base Solution due to a lack of sterility assurance. The products were compounded by Intrathecal Compounding Specialists.

    Product
    All sterile drug preparations remaining within expiry prepared from Sufentanil Citrate Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0556-2018·2018-02-14

    Recall of Emprint Percutaneous Antenna Due to Tip Disengagement

    FDA is recalling Emprint Percutaneous Antennas because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 15cm, Material CA15L1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0561-2018·2018-02-14

    FDA Recalls Covidien Emprint Percutaneous Antenna Due to Tip Disengagement

    FDA is recalling specific lots of the Covidien Emprint Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm (reinforced), Material CA30L2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0320-2018·2018-02-14

    FDA Recalls Fentanyl Citrate Sterile Drug Preparations for Sterility Concerns

    Intrathecal Compounding Specialist, LLC is recalling sterile drug preparations made from Fentanyl Citrate Base Solution due to a lack of sterility assurance.

    Product
    All sterile drug preparations remaining within expiry prepared from Fentanyl Citrate Base Solution dispensed between October 16, 2017 and November 17, 2017 Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0334-2018·2018-02-14

    Flawless Beauty Recalls Unapproved Saluta Glutathione Whitening Kits Nationwide

    Flawless Beauty LLC is voluntarily recalling all lots of Saluta Glutathione Whitening kits nationwide because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).

    Product
    Saluta Glutathione Whitening kits, packaged in 600 mg, 1200 mg and 1800 mg glass vials, Manufactured by: Shandong Luye Pharmaceutical Co, Ltd, Yantai, Shandong. PRC
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0803-2018·2018-02-14

    Daisho Kimchi Hot Pot Soup Base Recalled for Undeclared Fish Allergens

    JFC International is recalling Daisho Kimchi Hot Pot Soup Base because it contains undeclared shrimp and crab.

    Product
    Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported by JFC International Inc., Los Angeles, CA.
    Category
    Food
    Distribution
    28 states
  • HighNHTSA·18V109000·2018-02-14

    Lance Recalls 2018 Recreational Trailers Due to Power Tongue Jack Defect

    Lance is recalling 2018 recreational trailers because a power tongue jack touch pad may crack, allowing water entry and causing the jack to operate unintentionally.

    Product
    LANCE — LANCE 1995, 2465, 2185, 2285
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0795-2018·2018-02-14

    SunGlow Margarine Recalled for Undeclared Soy Lecithin

    Ventura Foods is recalling SunGlow European Style Butter Blend Margarine because it contains undeclared soy lecithin, a common allergen.

    Product
    SunGlow, European Style Butter Blend Margarine, packaged in the following configurations: 1. 16842 SNG, Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC 26700-13410. Outer case: Net Wt 36 lb (16.32 kg). UPC 1 00 26700 13410 1 Ventura Foods, Brea, CA 92821 2.…
    Category
    Food
    Distribution
    36 states
  • HighNHTSA·18V106000·2018-02-14

    Setra Recalls 2006-2010 S417 Buses Due to Door Pinch Hazard

    Setra is recalling 2006-2010 S417 buses because a doorway strip may fail to prevent pinch injuries from swiveling entry doors.

    Product
    SETRA — SETRA S417
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0531-2018·2018-02-14

    Angiodynamics Recalls Accu2i Microwave Tissue Ablation Applicators

    Angiodynamics, Inc. is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering the desired microwave energy.

    Product
    Accu2i pMTA Applicator, 19 cm INTERMEDIATE, REF/Catalog # 900-602-US, Model # (UPN) H787900602US0, STERILE --- This is only for use with a Sulis V Generator, REF 806-10. Product Usage: The Acculis Accu2i pMTA Microwave Tissue Ablation Applicator is indicated for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0329-2018·2018-02-14

    Flawless Beauty Recalls Unapproved Laennec Placenta Extract Injections

    Flawless Beauty LLC is voluntarily recalling Laennec INJ placenta extract vials because they were marketed without FDA approval.

    Product
    Laennec INJ, Placenta extract (human), 2mL vials, Manufactured by: GCJBP Corp, Korea
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0536-2018·2018-02-14

    Bard Access Systems Recalls PowerPICC Provena Catheters Due to Possible Leaks

    Bard Access Systems is recalling 53,699 PowerPICC Provena Catheters due to possible leaks at the luer hub extension leg junction.

    Product
    PowerPICC Provena Catheters, as 3 Fr. Single lumen and 4 Fr. Dual Lumen. Packaged in a poly tray with Tyvek lid within a header bag configuration or a breather bag configuration.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0751-2018·2018-02-14

    Palmer Candy Recalls Sea Salt Caramel Hearts Due to Undeclared Peanut

    Palmer and Company is recalling Sea Salt Caramel Hearts because a peanut was found on the packaging. Peanuts are not listed on the label.

    Product
    Sea Salt Caramel Hearts, Net Wt 12 OZ (340 g), Made by Palmer Candy Company, Sioux City, Iowa. UPC 77232-17091
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0530-2018·2018-02-14

    Angiodynamics Recalls Accu2i Microwave Tissue Ablation Applicators

    Angiodynamics is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering microwave energy.

    Product
    Accu2i pMTA Applicator, 29 cm LONG, REF/Catalog # 900-601-US, Model # (UPN) H787900601US0, STERILE --- This is only for use with a Sulis V Generator, REF 806-10. Product Usage: The Acculis Accu2i pMTA Microwave Tissue Ablation Applicator is indicated for the intraoperative…
    Category
    Medical Device
    Distribution
    Distributed nationwide