The Recall Desk

State

Nebraska product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53901–53925 of 78407

  • ModerateFDA (Devices)·Z-0614-2016·2016-01-13

    Siemens Acute Care CCRP TestPak Recalled for Barcode Scanning Issues

    Siemens Healthcare Diagnostics Inc is recalling 78 units of the Acute Care CCRP TestPak because barcode labels may not scan on Stratus CS systems.

    Product
    Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to be used for calibration of the CCRP method on the Stratus¿ CS analyzer Catalog Number: CCCRP SMN:10445066
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0562-2016·2016-01-13

    Freedom Pharmaceuticals Recalls Subpotent 5-methyltetrahydrofolate Calcium Drug

    Freedom Pharmaceuticals is voluntarily recalling specific lots of 5-methyltetrahydrofolate Calcium because the drug was found to be subpotent.

    Product
    5-methyltetrahydrofolate Calcium (L) (a) 1 gm in 2 oz container NDC: 52372-0855-04; (b) 5 gm in 2 oz container NDC: 52372-0855-02; (c) 25 gm in 4 oz container NDC: 52372-0855-02, Rx only; Manufactured by: Hangzhou Dayangchem Co., Ltd. 328 Wener Rd, Xihu, Hangzhou, Zhejiang…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0583-2016·2016-01-13

    Ultradent Recalls InterGuard Dental Refills Due to Manufacturing Defect

    Ultradent is recalling InterGuard 5.5mm Econo Refills because the floss tether hole was not completely punched through.

    Product
    InterGuard 5.5mm Econo Refill, sizes, 4.0mm for short anatomical crowns and 5.5mm, part # 4012 Product Usage: InterGuard is a preventive aid for operative dentistry. It is used to protect adjacent teeth from iatrogenic preparation damage. This includes cavity and tunnel…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E001000·2016-01-12

    Wells Recalls Brake Light Switches for Potential Failure to Illuminate

    Wells Vehicle Electronics is recalling specific brake light switches that may fail to illuminate brake lights or disengage cruise control, increasing crash risk.

    Product
    EXTERIOR LIGHTING:BRAKE LIGHTS:SWITCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16062·2016-01-12

    Walmart Recalls Rival Electric Griddles Due to Shock Hazard

    Walmart is recalling Rival brand electric griddles because the heating element can crack, allowing water to enter and posing a shock hazard.

    Product
    Rival brand griddles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V007000·2016-01-11

    Gulf Stream Motor Homes Recalled for Unstable Entry Steps

    Gulf Stream is recalling 662 motor homes because a bolt on the electric steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    GULF STREAM — GULF STREAM YELLOWSTONE, TOUR MASTER, TOY HAULER, CARIBBEAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V005000·2016-01-08

    Trans Tech School Bus Stop Arm Decal Recall

    Transportation Collaborative is recalling 257 model year 2015 Trans Tech school buses because a reflective decal on the stop arm may peel loose, reducing visibility.

    Product
    TRANS TECH — TRANS TECH, TRANS TECH BUS ROADSTAR, STUDENT SAFETY TRANSPORT, ST AERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·005-2016·2016-01-08

    New York Style Sausage Co. Recalls Pork Sausage Due to Undeclared Sheep Casings

    New York Style Sausage Co. is recalling approximately 4,040 pounds of pork sausage because the products use sheep casings that are not declared on the label, posing an allergy risk.

    Product
    NEW YORK STYLE SAUSAGE CO. — New York Style Sausage Co. Recalls Pork Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16C001000·2016-01-08

    Britax Recalls B-Safe 35 Child Seats Due to Handle Cracks

    Britax is recalling specific B-Safe 35 infant car seats because the carry handles may crack and fracture, posing a risk of injury if the seat falls.

    Product
    CHILD SEAT:HANDLE (INFANT) recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V006000·2016-01-08

    Blue Bird Recalls School Buses with Peeling Stop Arm Decals

    Blue Bird is recalling 2016-2017 Vision and All American school buses because stop arm reflective decals may peel off, reducing visibility to other drivers.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16069·2016-01-07

    Office Depot Recalls Crawley II Executive Chairs Due to Fall Hazard

    Office Depot is recalling Crawley II executive chairs because the seat plate weld can break, posing a fall hazard. No injuries have been reported.

    Product
    Crawley II Executive Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0441-2016·2016-01-06

    Tate's Bake Shop Recalls Cookies for Undeclared Walnuts

    Tate's Bake Shop is recalling Chocolate Chip and Ginger Zinger Cookies because they contain undeclared walnuts.

    Product
    TATE'S BAKE SHOP Cookies GINGER ZINGER GLUTEN FREE, NET WT. 7 OZ (198 G), UPC Code 810291001095, product is packed in plastic which is inserted into a mint green paper wrapper, DISTRIBUTED BY: TATE'S BAKE SHOP 43 NORTH SEA RD. SOUTHAMPTON NY 11968 631-780-6511…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0557-2016·2016-01-06

    Elekta Recalls MOSAIQ Oncology System Due to Dosage Calculation Error

    Elekta, Inc. is recalling 399 units of the MOSAIQ Oncology Information System because a software issue with age and weight data can cause incorrect drug dosages.

    Product
    MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be used wherever radiotherapy and/or chemotherapy are prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0440-2016·2016-01-06

    Tate's Bake Shop Recalls Chocolate Chip Cookies for Undeclared Walnuts

    Tate's Bake Shop is recalling Chocolate Chip Cookies and Ginger Zinger Cookies because they contain undeclared walnuts.

    Product
    TATE'S BAKE SHOP CHOCOLATE CHIP COOKIES, NET WT. 7 OZ (198 G), UPC Code 810291001002, product is packed in plastic which is inserted into green paper wrapping, DISTRIBUTED BY: TATE'S BAKE SHOP 43 NORTH SEA RD. SOUTHAMPTON NY 11968 631-780-6511, WWW.TATEBAKESHOP.COM, MADE IN THE…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0561-2016·2016-01-06

    Beckman Coulter MicroScan Pos Breakpoint Combo Panel Recall

    Beckman Coulter is recalling MicroScan Pos Breakpoint Combo Panel Type 20 due to falsely negative Voges-Proskauer results.

    Product
    MicroScan Pos Breakpoint Combo Panel Type 20, Part No. B1017-202 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0569-2016·2016-01-06

    BD Vacutainer PLUS K2EDTA Tubes Recalled for Insufficient Additive

    Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA tubes because they may contain insufficient EDTA additive, which can lead to erroneous platelet results.

    Product
    BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm x 3.0 mL (Lavender) BD Hemogard Additive: K2EDTA (spray dried), 5.4mg Sterile IVD BD, Made in USA BD Vacutainer¿ tubes are used to collect, transport and process blood in a closed system. These tubes are used for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2016·2016-01-06

    Neto's Sausage Recalls Meat and Poultry Products Labeled Without Inspection

    Neto's Sausage Co. is recalling approximately 7,687 pounds of beef, pork, and chicken products that were labeled with the federal mark of inspection without FSIS oversight.

    Product
    Silva Sausage Co. — Neto's Sausage Co., Inc. Recalls Meat and Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0568-2016·2016-01-06

    BD Vacutainer PLUS K2EDTA Tubes Recalled for Insufficient Additive

    Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA tubes because some were manufactured with insufficient EDTA additive, which may lead to erroneous platelet results.

    Product
    BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm x 2.0 mL (Pink) BD Hemogard Additive: K2EDTA (spray dried), 3.6mg Sterile IVD BD, Made in USA BD Vacutainer¿ tubes are used to collect, transport and process blood in a closed system. These tubes are used for testing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0570-2016·2016-01-06

    BD Vacutainer PLUS K2EDTA Tubes Recalled for Insufficient Additive

    Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA tubes because some were manufactured with insufficient EDTA additive, which may lead to erroneous platelet results.

    Product
    BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm x 3.0 mL (Tan) BD Hemogard Additive: K2EDTA (spray dried), 5.4mg Sterile IVD BD, Made in USA BD Vacutainer¿ tubes are used to collect, transport and process blood in a closed system. These tubes are used for testing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0559-2016·2016-01-06

    Beckman Coulter MicroScan Pos Combo Panel Recall for False Negative Results

    Beckman Coulter is recalling MicroScan Pos Combo panels that may produce falsely negative Voges-Proskauer results for Staphylococcus aureus.

    Product
    MicroScan Pos Combo Panel Type 33, Part No. B1017-211 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0563-2016·2016-01-06

    Trumpf Ceiling Mounted Surgical Light Systems Recalled for Falling Hazard

    Trumpf Medical Systems is recalling 20,713 ceiling-mounted surgical light systems because the spring arm can detach, causing the light head to fall.

    Product
    Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5
    Category
    Medical Device
    Distribution
    Distributed nationwide