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.

59351–59375 of 78413

SevereFDA (Devices)·Z-0953-2015·2015-01-21
DePuy ATTUNE INTUITION Impaction Handle Recalled for Fracture Risk
DePuy Orthopaedics is recalling ATTUNE INTUITION Impaction Handles because the lever can fracture during knee surgery, potentially leaving device pieces in the patient.
Product
The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized in knee replacement procedures. The instrument interfaces with several related ATTUNE instruments: keel punch, tibial tower, evaluation bullet, fixed bearing tibial impactor, rotating platform tibial…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0956-2015·2015-01-21
Brainlab iPlan RT Dose Software Recalled for Potential Positioning Errors
Brainlab AG is recalling iPlan RT Dose software because it may produce incorrect patient positioning when using multiple CT image data sets.
Product
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic, conformal, computer planned, Linac based radiation treatment of cranial, head and neck, and extracranial lesions.
Category
Medical Device
Distribution
45 states
HighCPSC·15716·2015-01-21
La-Z-Boy Recalls Silver Luxury Lift Chair Control Wands for Burn Hazard
La-Z-Boy is recalling control wands sold with Silver Luxury Lift Chairs because they can overheat and cause burns. Consumers should unplug the chair and contact a dealer for a free replacement.
Product
La-Z-Boy Control Wands sold with Silver Luxury Lift Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0957-2015·2015-01-21
Brainlab iPlan RT Software Recalled for Potential Incorrect Patient Positioning
Brainlab AG is recalling iPlan RT radiation treatment planning software due to a risk of incorrect patient positioning when using multiple localized CT image data sets.
Product
iPlan RT is a radiation treatment planning system that is intended for use in stereotactic, conformal, computer planned, Linac based radiation treatment of cranial, head and neck, and extracranial lesions.
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0974-2015·2015-01-21
Becton Dickinson Recalls Trypticase Soy Agar and MacConkey II Agar Plates
Becton Dickinson is recalling specific lots of Trypticase Soy Agar and MacConkey II Agar plates due to low-level Listeria monocytogenes contamination.
Product
TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar Trypticase Soy Agar with 5% Sheep Blood is used for the growth of fastidious organisms and for the visualization of hemolytic reactions. MacConkey II Agar is a selective and differential medium for the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0972-2015·2015-01-21
Siemens Artis Q Ceiling Systems Recalled for Cable Wear Risk
Siemens is recalling 50 Artis Q and Artis Q.zen ceiling systems because suboptimal cable routing may cause wear, leading to limited functionality or system failure.
Product
Artis Q, and Artis Q.zen ceiling systems; model numbers: 10848281; 10848354: The Artis family is dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0977-2015·2015-01-21
SpineFrontier Recalls Inline Persuader Pedicle Screw System Due to Handle Crack
SpineFrontier, Inc. is recalling four Inline Persuader PedFuse Pedicle Screw Systems because a crack may develop in the handle, potentially progressing with continued use.
Product
lnline Persuader- PedFuse Pedicle Screw System; Part Number: 11-80164
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0949-2015·2015-01-21
St. Jude Medical Merlin@home Transmitter Software Reset Recall
St. Jude Medical is recalling Merlin@home RF Remote Monitoring Transmitters because a software reset may cause backup operation in implanted cardiac devices.
Product
Merlin@home RF Remote Monitoring Transmitter, Model EX1150, with software versions 6.1M or 7.0. Usage:RF Remote Transmitter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0973-2015·2015-01-21
Synthes Malleable C-Retractor Recalled Due to Potential Spring Corrosion
Synthes, Inc. is recalling Malleable C-Retractors because the internal spring may corrode or fail, potentially transferring particles to patients and causing adverse tissue reactions or infection.
Product
Malleable C- Retractor, Part Number 397.232, used to provide retraction of the soft tissues during use of trocar instrumentation. Used in the following systems: the Basic Trocar System, Universal Trocar System, Craniofacial Modular Fixation System, Craniofacial (CMF)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0979-2015·2015-01-21
Philips CT Systems Recalled for Improper Vertical Motor Assembly
Philips is recalling Brilliance and Ingenuity CT systems because improper assembly of the vertical motor/brake system may lead to uncommanded vertical motion.
Product
Various Brilliance and Ingenuity Computed Tomography X-ray systems; one unit per package Product Usage: Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. This device may include…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·15061·2015-01-21
Mean Green Cleaner and Degreaser Recalled for Ammonia Mislabeling
CR Brands is recalling Mean Green cleaner and degreaser products because they may contain ammonia despite labels stating otherwise, posing a chemical hazard.
Product
Mean Green® Super Strength Cleaner & Degreaser and Mean Green® Industrial Strength Cleaner & Degreaser
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0976-2015·2015-01-21
Becton Dickinson Recalls Columbia Agar with 5% Sheep Blood Due to Listeria
Becton Dickinson & Co. is recalling Columbia Agar with 5% Sheep Blood due to low-level Listeria monocytogenes contamination. The product is a non-sterile culture medium distributed worldwide.
Product
Columbia Agar with 5% Sheep Blood Columbia Agar with 5% Sheep Blood is a general purpose culture medium used for the growth and recovery of fastidious microbial species.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0975-2015·2015-01-21
Becton Dickinson Recalls CDC Anaerobe Agar Due to Listeria Contamination
Becton Dickinson is recalling CDC Anaerobe 5% Sheep Blood Agar due to low-level Listeria monocytogenes contamination. The affected non-sterile media were distributed worldwide.
Product
CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Blood Agar is an enriched, nonselective culture medium particularly useful or the isolation and cultivation of obligate anaerobes from clinical specimens. It supports the growth of a wide variety of obligately anaerobic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0960-2015·2015-01-21
Siemens Symbia CT Systems Recalled for Internal Component Damage
Siemens Medical Solutions is recalling 295 Symbia T and T2 CT systems because a component may come loose and damage the equipment.
Product
Symbia T and Symbia T2 computer tomography systems. These systems are used to perform SPECT, CT, and SPECT + CT scans and imaging studies.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0947-2015·2015-01-21
Phadia 1000 Instrument Recalled for Rack Sequencing Error
Phadia US Inc is recalling 146 Phadia 1000 instruments due to a software error that may cause sample ID and test result mismatches.
Product
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since launch in 2003); Multiple ImmunoCAP assays for Allergen Testing, FDA Cleared for use on Phadia 1000 instrument with IU statement-see attachments. Software…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0981-2015·2015-01-21
Straumann Dental Implant Drill Set Recalled for Incorrect Drill
Straumann USA is recalling dental implant drill sets that may contain incorrect drills. The recall covers 362 pieces distributed nationwide and internationally.
Product
Drill set long, drill stop compatible for 4.8mm diameter implant, Article Number 040.447S Endosseous dental implant drill set.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0965-2015·2015-01-21
Biocare Medical Recalls MUM-1 Antibody Lots Due to Staining Intensity Issues
Biocare Medical is recalling three lots of MUM-1 antibody because staining intensity drops over time, potentially affecting diagnostic accuracy.
Product
MUM-1 (Multiple myeloma oncogene-1), catalog number PRM352 AA; Product Usage: For In Vitro Diagnostic Use. This antibody may be used as a tool for the identification and the sub classification of lymphoid malignancies : Multiple myeloma oncogene-1 (MUM-1) is a protein…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0969-2015·2015-01-21
Ortho VITROS 5600 System Recalled for Software Calibration Error
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because software may fail to identify expired calibrations.
Product
VITROS 5600 Integrated System, Catalog Number 6802413, IVD --- Ortho Clinical Diagnostics. For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products Slides, VITROS…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0968-2015·2015-01-21
Ortho VITROS 4600 Chemistry System Recalled for Software Calibration Error
Ortho-Clinical Diagnostics is recalling VITROS 4600 Chemistry Systems because software versions 3.1 and below may fail to identify expired calibrations.
Product
VITROS 4600 Chemistry System (VITROS 5,1 FS System family member), Catalog Number 6802445, IVD --- Ortho Clinical Diagnostics. The VITROS 4600 Chemistry System is intended for use in the in vitro quantitative measurement of a variety of analytes of clinical interest, using…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0988-2015·2015-01-21
Ziemer Femto LDV Z-Generation Lasers Recalled for Missing Starter Kits
Ziemer USA Inc. is recalling 26 Femto LDV Z-Generation femtosecond surgical lasers because they were not shipped with the required Starter Kits.
Product
Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0784-2015·2015-01-21
NatureBox Sweet Blueberry Almonds Recalled for Missing Soy Labeling
NatureBox, Inc. is recalling Sweet Blueberry Almonds because the product label failed to list soy lecithin, an ingredient included in the recipe.
Product
Sweet Blueberry Almonds - Blueberry Flavored Almonds. Ingredients: Almonds, Sugar, Natural Flavor, Vegetable Color (Red Cabbage Juice Extract), Beet Juice Concentrate. May also contain other tree nuts, peanuts, milk, wheat, egg. Packaged in the following configuration: 4…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0967-2015·2015-01-21
Ortho VITROS 3600 Immunodiagnostic System Recalled for Software Anomaly
Ortho-Clinical Diagnostics is recalling VITROS 3600 systems because software versions 3.1 and below may fail to identify expired calibrations.
Product
VITROS 3600 Immunodiagnostic System, Catalog Number 6802783, IVD --- Ortho Clinical Diagnostics. For use in the in vitro quantitative, semi-quantitative and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0986-2015·2015-01-21
Stryker Recalls SurgiCounter Charging Cradles Due to Charging Defects
Stryker is recalling 3,625 SurgiCounter Charging Cradles because they may fail to charge the scanner or download data after surgical procedures.
Product
The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging Cradles are designed to be used with the SurgiCounter and are part of the SurgiCount Safety-Sponge System. The SurgiCount Safety-Sponge System is indicated for use in counting and recording the number…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V016000·2015-01-20
Porsche Recalls 2011-2012 Hybrid Models Due to Fuel Leak Risk
Porsche is recalling 2011-2012 Cayenne S Hybrid and 2012 Panamera S Hybrid vehicles because the fuel injection system may leak, increasing fire risk.
Product
PORSCHE — PORSCHE PANAMERA S HYBRID, CAYENNE S HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V021000·2015-01-20
Polar Tank Trailer Recall for Potential Brake Fire Risk
Polar Tank Trailer is recalling 2015 ATB6, APX0, and SRJH trailers due to a parking brake actuator defect that may cause brake drag and fire.
Product
POLAR TANK — POLAR TANK ATB6 TRAILER, APX0 TRAILER, SRJH TRAILER
Category
Vehicle
Distribution
Distributed nationwide