The Recall Desk

State

Nebraska product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36601–36625 of 78318

  • ModerateFDA (Devices)·Z-1134-2019·2019-04-24

    Ethicon Recalls VICRYL Sutures Due to Labeling Mismatch

    Ethicon, Inc. is recalling VICRYL, VICRYL Plus, and PDS sutures because the product may not match the sales unit carton and foil label.

    Product
    VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM) 4-0 UND VICRYL SUTURE 18"(45CM) 2-0 VIO VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM) 2-0 VIO VICRYL CT VIO 8X18IN 0 S/A CT-1 CR VICRYL SUTURE 18"(45CM) 1 VIO VCL CT UD 8X18IN 2-0 S/A CP-2 CR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1301-2019·2019-04-24

    ConAgra Recalls Hunts Tomato Paste Cans Due to Potential Mold

    ConAgra Foods is recalling 145,380 cans of Hunts Tomato Paste No Salt Added due to potential mold caused by can damage.

    Product
    Hunts Tomato Paste No Salt Added 6 ounce cans, 12 per wholesale tray Can UPC: 2700038807 Tray UPC: 2700038809
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1140-2019·2019-04-24

    Philips Medical Systems Recalls Foot Switches for Imaging Systems

    Philips Medical Systems is recalling 7,209 foot switches used with specific imaging systems because bent pedals may prevent live fluoroscopy images or exposures.

    Product
    Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 Product The Allura Xper FD Series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1164-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences Corp. is recalling Talar Dome Total Ankle Prostheses because the labels list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Flat Cut, Size 3, Left, Product No. LJU823T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1195-2019·2019-04-24

    Siemens syngo Lab Data Manager System Recalled for Software Issues

    Siemens Healthcare Diagnostics is recalling 449 syngo Lab Data Manager systems due to software issues. The recall covers systems distributed in the US and nine other countries.

    Product
    syngo Lab Data Manager System - Product Usage: syngo Lab Data Manager is a clinical system that assists medical laboratory professions with pre-analytic and post-analytic functions. It works in conjunction with multiple instruments, the laboratory information system (LIS) and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1163-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Flat Cut, Size 2, Left, Product No. LJU822T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1170-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Right, Product No. LJV182T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1194-2019·2019-04-24

    Roche Albumin BCP Reagent Recalled for Calibration Failures and QC Imprecision

    Roche Diagnostics is recalling 774 units of Albumin BCP reagent due to calibration failures and QC imprecision caused by elevated pH levels.

    Product
    Albumin BCP Product Usage: ALBP is an in vitro test used for the quantitative determination of albumin in human serum and plasma on Roche/Hitachi cobas c systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1124-2019·2019-04-24

    InvaGen Recalls Testosterone Cypionate Injection Due to Particulate Matter

    InvaGen Pharmaceuticals is recalling specific lots of Testosterone Cypionate Injection because of the presence of particulate matter. The affected vials were distributed nationwide.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1165-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.

    Product
    Talar Dome Total Ankle Prosthesis , Flat Cut, Size 1, Right, Product No. LJU811T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1172-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Left, Product No. LJV190T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1153-2019·2019-04-24

    Integra Recalls Salto Talaris Ankle Prosthesis Due to Labeling Error

    Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels list an incorrect metallic coating material symbol.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 3, Right, Part No. LJU203T
    Category
    Medical Device
    Distribution
    26 states
  • LowFDA (Drugs)·D-1252-2019·2019-04-24

    Johnson Matthey Recalls Remifentanil HCl API Due to Impurity Issues

    Johnson Matthey Inc. is recalling Remifentanil HCl active pharmaceutical ingredient (API) because an unknown impurity exceeded specification limits.

    Product
    Remifentanil HCl active pharmaceutical ingredient (API) for manufacturing, processing or repackaging, 416.95 g glass container, Rx ONLY, Johnson Matthey Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, NJ 08066-1742.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1198-2019·2019-04-24

    Cordis Guiding Catheters Recalled for Frayed Mounting Card Fragments

    Cordis Corporation is recalling Vista Brite Tip and Androit guiding catheters because frayed pieces of the mounting card were found inside the primary packaging.

    Product
    Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1132-2019·2019-04-24

    Estee Lauder Recalls Repairwear Cream Due to Ineffective Container Seal

    Estee Lauder Inc is recalling 14,490 jars of Repairwear Laser Focus Line Smoothing Cream SPF 15 because the seal between the cap and jar is ineffective.

    Product
    Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar with a silver cap, Clinique Laboratories, Dist. New York, NY 10022
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V319000·2019-04-23

    Toyota Recalls 2015-2017 Yaris Vehicles for Air Bag Wire Harness Defect

    Toyota is recalling 2015-2017 Yaris vehicles because wire harnesses for side air bag sensors may crack and corrode, potentially causing air bags to fail to deploy or deploy improperly.

    Product
    TOYOTA — TOYOTA YARIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V318000·2019-04-23

    Toyota Recalls 2019 Sienna Vehicles Due to Passenger Air Bag Sensor Defect

    Toyota is recalling 2019 Sienna vehicles because incorrect welds in the passenger front door may affect air bag sensor readings, potentially causing unintended deployment or failure to deploy.

    Product
    TOYOTA — TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V320000·2019-04-23

    Jeep Wrangler Recall for Roof Top Tent Cover Detachment Risk

    American Fastbacks is recalling 2018 Jeep Wranglers with roof top tents because the cover may crack and detach while driving, creating a road hazard.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19T004000·2019-04-22

    Toyo Recalls Proxes A27 Tires Due to Tread Detachment Risk

    Toyo is recalling specific Proxes A27 tires where a rubber compound error may cause tread to detach, increasing crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V317000·2019-04-19

    Forest River Recalls 2019 Rockwood and Flagstaff Trailers for Fire Risk

    Forest River is recalling 2019 Rockwood and Flagstaff recreational trailers because improperly installed air conditioning wiring may contact a heat strip, increasing the risk of fire.

    Product
    FOREST RIVER — FOREST RIVER FLAGSTAFF, ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V315000·2019-04-18

    Honda Recalls 2017-2018 Clarity Fuel Cell Vehicles for Water Pump Defect

    Honda is recalling 2017-2018 Clarity Fuel Cell vehicles because internal corrosion may cause the water pump to fail, potentially leading to a vehicle stall and increased crash risk.

    Product
    HONDA — HONDA CLARITY FUEL CELL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V314000·2019-04-18

    Mercedes-Benz Recalls 2019 A 220 Vehicles Due to Brake Pedal Welding Defect

    Mercedes-Benz is recalling 2019 A 220 and A 220 4MATIC vehicles because improper welding may cause the pedal plate to bend, impairing brake pedal operation and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ A 220
    Category
    Vehicle
    Distribution
    Distributed nationwide