The Recall Desk

State

Nebraska product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50026–50050 of 78397

  • SevereFDA (Devices)·Z-2768-2016·2016-09-14

    Bayer Certegra Workstation Recalled for Fire and Smoke Risk

    Bayer Healthcare is recalling 165 Certegra Workstations used with Medrad Stellant CT Injection Systems because they may produce smoke and sparks of fire.

    Product
    Certegra Workstation used in conjunction with Medrad Stellant CT Injection System Catalog Number # CWKS DISPLAY Serial Numbers The Medrad Stellant CT Injector System is intended for the specific purpose of injecting intravenous contrast media into humans for diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2069-2016·2016-09-14

    Nature Made Adult Gummies Recalled for Possible Salmonella Contamination

    Pharmavite is recalling specific lots of Nature Made adult gummies due to possible Salmonella contamination. Consumers should check lot numbers and stop using the product.

    Product
    Nature Made(R) adult gummies Multi for Her plus Omega-3, 150 count, UPC 0-31604-04275-2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2080-2016·2016-09-14

    Lysander's Spicy Bourbon Rub Recalled for Undeclared Soy and Wheat Allergens

    Geneva Foods is recalling Lysander's All Natural Spicy Bourbon Flavor Rub because it contains undeclared soy and wheat allergens and does not declare sulfites.

    Product
    Lysander's All Natural Spicy Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g) foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2099-2016·2016-09-14

    Dannon Recalls Activia Fiber Yogurt Due to Incorrect Gluten-Free Labeling

    The Dannon Company is recalling Activia FIBER Lowfat Yogurt because the packaging displays a Certified Gluten-Free mark despite containing wheat.

    Product
    Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packaged in form fill seal plastic cups
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-2722-2016·2016-09-14

    Hospira Recalls Plum A+ Infusion Pumps Due to Undersized Diaphragm

    Hospira Inc. is recalling 357,778 Plum A+ Hyperbaric Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruptions.

    Product
    Plum A+ Hyperbaric Infusion Pump. List Number 11005. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2736-2016·2016-09-14

    Philips BrightView XCT Gamma Camera Recalled for Software Defect

    Philips Medical Systems is recalling 424 BrightView XCT gamma cameras due to a software defect that may cause the detector to contact patients during specific scans.

    Product
    BrightView XCT Model 882482, gamma camera for Single Photon Emission Computed Tomography (SPECT)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2745-2016·2016-09-14

    Smith & Nephew Whipknot Soft Tissue Cinch Suture Recalled for Sterility Breach

    Smith & Nephew is recalling Whipknot Soft Tissue Cinch sutures because sterile packaging was breached, compromising sterility. The recall covers 34,065 units distributed worldwide.

    Product
    Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: 7211015 Used during ligament reconstruction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16262·2016-09-14

    Zeagle Buoyancy Control Devices Recalled for Drowning Hazard

    Huish Outdoors is recalling Zeagle Grace and Element BCDs because they may leak air, causing loss of flotation and posing a drowning risk to scuba divers.

    Product
    Zeagle brand buoyancy control devices (BCDs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2761-2016·2016-09-14

    Riverpoint Medical Recalls Nylon Surgical Sutures Due to Seal Integrity Issues

    Riverpoint Medical is recalling sterile nylon surgical sutures because the seals may become open during distribution or packaging.

    Product
    Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: 663BK 663BL 664BL 928BK Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2728-2016·2016-09-14

    Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm

    Hospira is recalling 357,778 Plum A+3 Infusion Pump Systems because an undersized fluid shield diaphragm may cause alarms and interrupt therapy.

    Product
    Plum A+3 Infusion Pump System. List Number 12348. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2068-2016·2016-09-14

    Nature Made Gummy Multivitamin Recalled for Possible Salmonella Contamination

    Pharmavite is recalling specific lots of Nature Made adult gummy multivitamins due to possible Salmonella contamination. Consumers should check their lot numbers and expiration dates.

    Product
    Nature Made(R) adult gummies Multi for Her plus Omega-3, 100 count, UPC 0-31604-04236-3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2098-2016·2016-09-14

    McCain Foods Recalls Fire Roasted Poblano and Jalapeno Popper Bites

    McCain Foods USA is recalling Fire Roasted Poblano & Jalapeno popper bites because the flour used was contaminated with E. Coli O121.

    Product
    Fire roasted Poblano & Jalapeno popper bites packaged in a white box with black lettering. The product is labeled in part: Canchor Poppers Fire Roasted & Jalapeno popper bites, 2-4 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2724-2016·2016-09-14

    Hospira Recalls Plum A+ Infusion Pumps Due to Undersized Diaphragm

    Hospira is recalling 357,778 Plum A+ Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and delay or interrupt therapy.

    Product
    Plum A+ Infusion Pump. List Number 11973. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2721-2016·2016-09-14

    Elekta Medical Linear Accelerator Recall for Loose Drive Gear Joint

    Elekta is recalling 553 Medical Linear Accelerators because a loose joint between the drive gear and gantry base drive wheel can lead to fatigue failure of securing bolts.

    Product
    Medical Linear Accelerator
    Category
    Medical Device
    Distribution
    20 states
  • HighFDA (Devices)·Z-2730-2016·2016-09-14

    Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm

    Hospira is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruption.

    Product
    Plum A+3 Infusion Pump with Hospira MedNet Software. List Number 20678. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2723-2016·2016-09-14

    Hospira Recalls Plum A+ Infusion Pumps Due to Undersized Diaphragm

    Hospira Inc. is recalling 357,778 Plum A+ Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruption.

    Product
    Plum A+ Infusion Pump. List Number 11971. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1485-2016·2016-09-14

    Amerisource Recalls Mispackaged Amphetamine Tablets Due to Dosing Errors

    Amerisource Health Services is recalling 156 cartons of 30 mg amphetamine tablets because blister cavities may contain more than one tablet.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 30 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2726-2016·2016-09-14

    Hospira Recalls Plum A+ Infusion Pumps Due to Undersized Diaphragm

    Hospira Inc. is recalling 357,778 Plum A+ Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and interrupt therapy.

    Product
    Plum A+ Infusion Pump with Hospira MedNet Software. List Number 20679. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2766-2016·2016-09-14

    Hologic Recalls SureSight Obturator Introducer Localization Systems Due to Tip Breakage

    Hologic is recalling 535 units of SureSight Obturator Introducer Localization Systems because the tip may break at the glue joint.

    Product
    SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI. ILS-0914-12-OB (9G Introducer Localization Set (OB Model) for ATEC0914-12MR Handpiece Product Usage: The Sure Sight Obturator Introducer Localization System (ILS-OB) is a Hologic accessory kit. It is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V666000·2016-09-14

    Freightliner Trucks Recalled for Incorrect Brake Malfunction Indicator Label

    Daimler Trucks is recalling 2016-2017 Freightliner trucks because the brake malfunction light may display 'PARK' instead of 'BRAKE', potentially hiding a braking issue.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC BUSINESS CLASS M2, S2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V663000·2016-09-14

    Smeal Recalls 2015-2016 Aerial Fire Apparatus Due to Touchscreen Defect

    Smeal is recalling 2015-2016 Aerial fire apparatus vehicles because touchscreen false activations may turn accessories on or off, increasing crash risk.

    Product
    SMEAL — SMEAL AERIAL FIRE APPARATUS, AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2097-2016·2016-09-14

    McCain Breaded Stuffed Jalapeno Poppers Recalled for E. Coli O121 Contamination

    McCain Foods USA is recalling breaded stuffed jalapeno poppers because the flour used in the product was contaminated with E. Coli O121.

    Product
    Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta Bold Poppers, breaded stuffed jalapenos, keep frozen. The product is packaged in a green 4 lb. box with white, green and orange lettering.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2735-2016·2016-09-14

    Philips BrightView X Gamma Camera Recalled for Software Defect

    Philips Medical Systems is recalling 117 BrightView X gamma cameras due to a software defect that may cause the detector to contact patients during specific scans.

    Product
    BrightView X, model #882478; gamma camera designed for single or dual detector nuclear imaging
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V661000·2016-09-14

    Honda Recalls 2014-2015 Grom and NSS300 Motorcycles for Fuel Pump Defect

    Honda is recalling 2014-2015 Grom 125 and NSS300 motorcycles because a resin bracket in the fuel pump may swell and seize, causing the engine to stall and increasing crash risk.

    Product
    HONDA — HONDA GROM125, NSS300
    Category
    Vehicle
    Distribution
    Distributed nationwide