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.

57326–57350 of 78413

HighFDA (Food)·F-2360-2015·2015-06-10
Amy's Vegetable Lasagna Recalled for Listeria Contamination
Amy's Kitchen is recalling Vegetable Lasagna, Light in Sodium, because a supplier notified them that spinach used in the product contained Listeria monocytogenes.
Product
Amy's Vegetable Lasagna, Light in Sodium, 9.5 oz (269 g) 12 boxes per case. UPC: 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2358-2015·2015-06-10
Amy's Stuffed Pasta Shells Recalled Due to Listeria Contamination
Amy's Kitchen is recalling Stuffed Pasta Shells Bowls because supplier-confirmed Listeria monocytogenes was found in spinach used in manufacturing.
Product
Amy's Stuffed Pasta Shells Bowl, 10.0 oz (284 g) 12 boxes per case. UPC: 0-42272-00178-1, US distribution only Amy Kitchen, Petaluma, CA
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1712-2015·2015-06-10
Elekta Oncentra Brachy software recalled for incorrect dose calculation errors
Elekta, Inc. is recalling Oncentra Brachy radiation therapy planning software because it may calculate incorrect doses for specific regions of interest.
Product
Oncentra Brachy radiation therapy planning software designed to analyze and plan radiation treatments in three dimensions for the purpose of treating patients with cancer.
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-1704-2015·2015-06-10
Siemens syngo Workflow SLR Recalled for Potential Order Loss
Siemens Medical Solutions USA is recalling 131 syngo Workflow SLR systems because a software defect may cause order loss during restarts, leading to diagnosis delays.
Product
syngo Workflow SLR; The information system syngo Workflow SLR is a digital radiology information system (RIS) with integrated modules for patient administration, examination, reporting, statistics and system administration. The system electronically displays stores, retrieves…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2355-2015·2015-06-10
Amy's Enchilada Verde Recalled Due to Listeria Contamination
Amy's Kitchen is recalling Enchilada Verde products because a spinach supplier notified them that the ingredient contained Listeria monocytogenes.
Product
Amy's Enchilada Verde Whole Meal, Spinach and Cheese 10.0 oz (284 g) 12 boxes per case. UPC: 0-42272-00085-2, US distribution only 8 pack, UPC: 0-42272-00085-2 - US Distribution Amy Kitchen, Petaluma, CA
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2353-2015·2015-06-10
Amy's Garden Vegetable Lasagna Recalled Due to Listeria Contamination
Amy's Kitchen is recalling Garden Vegetable Lasagna because supplier-confirmed Listeria monocytogenes was found in spinach used during manufacturing.
Product
Amy's Garden Vegetable Lasagna, 10.30 oz (291 g) 12 boxes per case. UPC: 0-42272-00041-8, US distribution only Amy's Kitchen, Petaluma, CA
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2351-2015·2015-06-10
Amy's Vegetable Lasagna Recalled Due to Listeria Monocytogenes Contamination
Amy's Kitchen is recalling Vegetable Lasagna products because supplier-confirmed Listeria Monocytogenes was found in spinach used in manufacturing.
Product
Amy's Vegetable Lasagna, 9.5 oz (269 g) 12 boxes per case. UPC 0 42272 00032 6 - US Distribution: UPC 0-42272-90032-9 - Canadian distribution Vegetable Lasagna 8 pack - 9.5 oz, (269g) UPC: 0-42272-00032-6 - US distribution Family Size, 28 oz. (794 g), 8 boxes per case…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1701-2015·2015-06-10
Zimmer CAS Recalls Tibial Alignment Guides Due to Spike Breakage Risk
Zimmer CAS is recalling 78 Tibial Alignment Guides because spikes may bend or break during use.
Product
Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2352-2015·2015-06-10
Amy's Tofu Vegetable Lasagna Recalled Due to Listeria Contamination
Amy's Kitchen is recalling Tofu Vegetable Lasagna because a supplier notified them that spinach used in the product contained Listeria monocytogenes.
Product
Amy's Tofu Vegetable Lasagna, 9.5 oz (269 g) 12 boxes per case. UPC 0-42272-00033-3, US distribution only Amy's Kitchen, Petaluma, CA
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2363-2015·2015-06-10
Amy's Gluten Free Vegetable Lasagna Recalled for Listeria Risk
Amy's Kitchen is recalling Gluten Free Vegetable Lasagna because supplier-confirmed Listeria monocytogenes was found in spinach used in the product.
Product
Amy's Gluten Free Vegetable Lasagna, 4.7 oz. 6 boxes per case. Amy Kitchen, Petaluma, CA
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2359-2015·2015-06-10
Amy's Gluten Free Tofu Scramble Breakfast Wraps Recalled for Listeria
Amy's Kitchen is recalling Gluten Free Tofu Scramble Breakfast Wraps because a spinach supplier notified them that the ingredient contained Listeria monocytogenes.
Product
Amy's Gluten Free Tofu Scramble Breakfast Wraps, 5.5 oz 156 g) 12 boxes per case. UPC: 0-42272-00807-0, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2361-2015·2015-06-10
Amy's Brown Rice & Vegetables Bowl Recalled for Listeria Risk
Amy's Kitchen is recalling Brown Rice & Vegetables Bowls because a supplier notified them that spinach used in manufacturing contained Listeria monocytogenes.
Product
Amy's Brown Rice & Vegetables Bowl, Light in Sodium, 9.5 oz (269 g) 12 boxes per case. UPC: 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1694-2015·2015-06-10
Zimmer Recalls 4.5mm Cortical Screws for M/DN Intramedullary Nail System
Zimmer, Inc. is recalling 4.5mm Cortical Screws for the M/DN system because they are not compatible with the device, potentially causing surgical complications.
Product
Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail System, Orthopedic surgical device.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1702-2015·2015-06-10
Alcon Custom Pak Recalled for Potential Glove Splits and Holes
Alcon Research, Ltd. is recalling Alcon Custom Paks because the Devon Light Glove component may have splits or holes, which could lead to surgical site infections.
Product
The Alcon Custom Pak. The Alcon Customer Pak is an assemblage of single-use medical devices and accessories designed by medical professionals for specific ophthalmic surgical procedures. Some Paks contain the Devon Light Glove.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15C002000·2015-06-10
Baby Jogger Recalls Infant Car Seats Due to Labeling Errors
Baby Jogger is recalling specific infant car seats because labels and manuals contain incorrect or missing safety information, which may increase injury risk in a crash.
Product
CHILD SEAT recall
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1113-2015·2015-06-10
Sucrets Cherry Lozenges Recalled for Incorrect Labeling
Medtech Products is recalling Sucrets Sore Throat & Cough Vapor Cherry lozenges because an incorrect book label was applied to the tins.
Product
SUCRETS Sore Throat & Cough Vapor Cherry lozenges, 18-count tin, Dist. By: Insight Pharmaceuticals, LLC, Trevose, PA 19053-8433
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1700-2015·2015-06-10
Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Heparin Activity Failure
Edwards Lifesciences is recalling 978 Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters because they failed internal statistical tests for heparin activity.
Product
Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters model number 744HF75. Flow-directed pulmonary artery catheters for monitoring cardiac output, mixed venous oxygen saturation, and end diastolic volume when used with the Vigilance Monitor.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1111-2015·2015-06-10
Mylan Recalls Mycophenolic Acid Tablets for Dissolution Failures
Mylan Pharmaceuticals is recalling 7,722 bottles of Mycophenolic Acid Delayed-release Tablets, 180 mg, because they failed to meet dissolution specifications.
Product
Mycophenolic Acid Delayed-release Tablets, 180 mg, 120-count bottle, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A., NDC 0378-4201-78, UPC 3 0378-4201-78 7.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1708-2015·2015-06-10
Siemens Dimension Vista LOCI TSH Test Recalled for Inaccurate Results
Siemens is recalling 2,256 units of the Dimension Vista LOCI TSH test due to a defect that may cause falsely low results.
Product
Dimension Vista Systems LOCI Thyroid Stimulating Hormone; the TSH method is an in vitro diagnostic test for the quantitative measurement of Thyroid Stimulating Hormone in human serum and plasma on the Dimension Vista System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1705-2015·2015-06-10
Siemens Medical Software Recall for Missing Image Measurements on Printouts
Siemens Medical Solutions is recalling 167 units of Syngo.via and Syngo.x software because measurements on subsequent images do not appear on printouts.
Product
Syngo.via and Syngo.x ; a software solution intended to be used for viewing, manipulation, communication, and storage of medical images.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1112-2015·2015-06-10
Teva Recalls Zebeta Tablets Due to Failed Dissolution Specifications
Teva Pharmaceuticals is recalling 889 bottles of Zebeta (bisoprolol fumarate) 10mg tablets because they failed dissolution specifications during stability testing.
Product
Zebeta¿ (bisoprolol fumarate), tablets, 10mg, 30-count bottle, Rx only, Manufactured for Teva Pharmaceuticals Inc. 425 Privet Road, Horsham, PA by Duramed Pharmaceuticals, Inc., a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY 10970 for Teva. NDC 51285-061-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1114-2015·2015-06-10
Fresenius Kabi Recalls KABIVEN IV Bags Due to Amino Acid Labeling Error
Fresenius Kabi is recalling 5,488 bags of KABIVEN IV solution because the label lists 3.1% amino acids, but the product actually contains 3.3%.
Product
KABIVEN — KABIVEN (DEXTROSE, SOYBEAN OIL, ELECTROLYTES, LYSINE, PHENYLALANINE, LEUCINE, VALINE, THREONINE, METHIONINE, ISOLEUCINE, TRYPTOPHAN, ALANINE, ARGININE, GLYCINE, PROLINE, HISTIDINE, GLUTAMIC ACID, SERINE, ASPARTIC ACID AND TYROSINE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1115-2015·2015-06-10
Sandoz Recalls Cetirizine HCl Chewable Tablets Due to Impurity Failure
Sandoz, Inc. is recalling specific lots of Cetirizine HCl Chewable Tablets because an impurity exceeded specifications during stability testing.
Product
Cetirizine HCl Chewable Tablet, 10 mg, 6-tablets in one blister, in 12 (2 blisters) and 24 (4 blisters) tablet count configurations. Manufactured by Sandoz Private Limited Village-Digham Opp. Thane-Belapur Road Navi Mumbai, 400 078, India, for Sandoz Private Limited 100 College…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1707-2015·2015-06-10
Ortho-Clinical Diagnostics Recalls VITROS Signal Reagent Due to Labeling Defects
Ortho-Clinical Diagnostics is recalling VITROS Immunodiagnostic Products Signal Reagent, Lot 3082, because the reagent packs may contain blank labels.
Product
VITROS Immunodiagnostic Products Signal Reagent, Product Code 1072693, Unique Device Identifier No. 10758750008360 VITROS Immunodiagnostics Products Signal Reagent (SR) is supplied to users as a sales unit box containing two Signal Reagent Packs. Each Signal Reagent Pack is…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V358000·2015-06-09
GM Recalls 2015 Cadillac ATS and CTS for Brake Pedal Bracket Fracture
General Motors is recalling 2015 Cadillac ATS and CTS vehicles because a brake pedal bracket may fracture, preventing the driver from applying the brakes.
Product
CADILLAC — CADILLAC CTS, ATS
Category
Vehicle
Distribution
Distributed nationwide