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.

57451–57475 of 78413

SevereFDA (Devices)·Z-1641-2015·2015-05-27
Ethicon Endo-Surgery Recalls Echelon Vascular White Reloads Due to Staple Line Defect
Ethicon Endo-Surgery is recalling 6,744 Echelon Vascular White Reloads because an internal inspection found a production issue that may cause the cartridge to deploy an incomplete staple line.
Product
ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip, Product Usage: The instruments have application in multiple open or minimally invasive general, gynecologic, urologic, thoracic and pediatric surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-2283-2015·2015-05-27
Fetting's Cinnamon Roll Dough Recalled for Missing Soy Ingredient Label
Top Taste, Inc. is recalling Fetting's Jumbo Cinnamon Roll Dough because the packaging failed to list defatted soy flour as an ingredient.
Product
Fetting's Jumbo 2.5 oz Cinnamon Roll Dough 140, Approx. 120 count, Keep Frozen, NET WT 18.8 LB., UPC 0 75812 79140 0, Packaged in plastic liner in cardboard box, Manufactured by Top Taste Inc, Finley, ND 58230..
Category
Food
Distribution
6 states
SevereFDA (Food)·F-2314-2015·2015-05-27
Waymouth Farms Recalls Raw Pine Nuts Due to Salmonella Risk
Waymouth Farms is recalling specific brands and sizes of raw pine nuts because they may be contaminated with Salmonella.
Product
Raw Pine Nuts sold in the following brands and package sizes: -Good Sense 3 oz. (85g) bag UPC 30243-86681, -Good Sense 4 oz. (113g) bag, UPC 30243-86680, -Good Sense 4 oz. (113g) tub UPC 30243-50799, -Good Sense 15 oz. (425g) bag UPC 30243-86687, -Good Sense 5…
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·15V316000·2015-05-27
Eldorado Axess, XHF, and E-Z Rider II Recalled for Engine Fire Risk
Eldorado is recalling 2007-2015 Axess, XHF, and E-Z Rider II vehicles because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.
Product
ELDORADO — ELDORADO E-Z RIDER II, AXESS, XHF
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V317000·2015-05-27
Keystone and Dutchmen Recalling 2015 Fifth Wheels for Expanding Room Defect
Keystone RV Company is recalling 2015 Keystone and Dutchmen fifth wheels because screws securing the expanding room may fail, increasing crash risk.
Product
DUTCHMEN — DUTCHMEN, KEYSTONE KODIAK, AEROLITE, CARBON, ALPINE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-2185-2015·2015-05-27
Superior Foods Recalls Organic Chopped Spinach Due to Possible Listeria Contamination
Superior Foods is recalling Simply Balanced Organic Chopped Spinach due to possible Listeria contamination. Consumers should not eat the product and should return it to the store.
Product
Simply Balanced Organic Chopped Spinach NET WT 10 OZ (283g) steam-in-bag Needs to be fully cooked Keep frozen
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1643-2015·2015-05-27
Philips Pinnacle3 Software Recall Due to Incorrect Dose Calculation
Philips Medical Systems is recalling Pinnacle3 software version 10.0 because a defect in the dose engine may cause incorrect radiation therapy dose calculations.
Product
Pinnacle3 Software Version 10.0, Model 459800200841. Product Usage: The Pinnacle 3 RTP software allows qualified medical professionals to enter patient data into the system, use that data to construct a plan for radiation therapy and evaluate the plan. Optionally, the…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V314000·2015-05-27
Crane Carrier Recalls 2008-2015 Trucks Due to Engine Fire Risk
Crane Carrier is recalling 630 model year 2008-2015 COE, LDT2, and LET2 trucks because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.
Product
CRANE — CRANE COE, LET2, LDT2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1639-2015·2015-05-27
Richard Allan Scientific Recalls Mucolytic Agent Due to Fungal Contamination
Richard Allan Scientific is recalling Mucolytic Agent and Mucolexx after a customer complaint reported fungal contamination in two lots of Mucolexx.
Product
Mucolytic Agent 1 pint/473 ml; 1 gallon/3.8 l Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology specimens. Mucolexx & Mucolytic Agent liquefies mucus and allows for optimal cytologic diagnostic results.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1628-2015·2015-05-27
Baxter ABACUS Software Recalled for Potential TPN Formula Loading Errors
Baxter is recalling ABACUS SE and ME software because it may load incorrect total parenteral nutrition formulas when duplicate order numbers are used.
Product
ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation Edition) Product Usage: The ABACUS Software is a Windows-based order entry software application for comprehensive total parenteral nutrition (TPN) calculations and label printing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1642-2015·2015-05-27
DeRoyal Specimen Retrieval Bags Recalled for Tearing During Use
DeRoyal Industries is recalling 5,359 Medium Specimen Retrieval Bags because they may tear or come apart during laparoscopic procedures.
Product
DeRoyal(R) Medium Specimen Retrieval Bag, REF 5500-000-003, Rx Only Product Usage: The device is a single-use specimen retrieval bag indicated for use in laparoscopic procedures to capture and remove organs or tissue from the body cavity.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1622-2015·2015-05-27
Roche Homocysteine Test System Recalled for Inaccurate Low Results
Roche Diagnostics is recalling Homocysteine Reagent lots due to complaints of under-recovery and falsely low patient results, which could delay diagnosis of peripheral vascular disease.
Product
Homocysteine test system - Homocysteine Reagent. 05385415190; Homocysteine 100 Tests, cobas c, COBAS INTEGRA Homocysteine Enzymatic Assay is an in vitro test for the quantitative determination of total L-homocysteine in human serum and plasma on Roche/Hitachi cobas c…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V315000·2015-05-27
Toyota Recalls 2015 Tundra for Incorrect Tire Pressure Placard
Southeast Toyota Distributors is recalling 144 model year 2015 Toyota Tundra vehicles because the tire placard lists incorrect inflation pressure, which could lead to underinflation and tire failure.
Product
TOYOTA — TOYOTA TUNDRA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1640-2015·2015-05-27
Richard-Allan Scientific Recalls Mucolexx Mucolytic Agent Due to Fungal Contamination
Richard-Allan Scientific is recalling Mucolexx mucolytic agent and Mucolexx products after a customer reported fungal contamination in two lots.
Product
Lerner Laboratories Mucolexx, 1 pint / 473 ml & 1 gallon/3.8 L; Shandon Mucolexx 500ml/0.13gal, 4L/1.06 gal, 120mL Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology specimens. Mucolexx & Mucolytic Agent liquefies mucus…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1634-2015·2015-05-27
Stryker Scorpio femoral component recall due to blister seal strength
Stryker Howmedica Osteonics is recalling 1,147 Scorpio femoral components because the inner blister peel strength may be below validated requirements, potentially affecting sterile barrier shelf life.
Product
Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1635-2015·2015-05-27
Stryker Triathlon Femoral Component Recalled for Sterile Barrier Seal Issues
Stryker Howmedica Osteonics is recalling 1,147 Triathlon femoral components because the inner blister seal strength may be below validated requirements, potentially affecting sterile shelf life.
Product
Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1633-2015·2015-05-27
Stryker Howmedica Hip Prosthesis Components Recalled for Seal Defects
Stryker Howmedica is recalling 1,147 RESTORATION Acetabular Augment System components because the inner blister seal strength may be below validated requirements, potentially affecting sterile shelf life.
Product
Stryker Howmedica Osteonics RESTORATION Acetabular Augment System; Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. Hip prosthesis component. The RESTORATION Acetabular Wedge Augments provide multiple options to address the wide range of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1626-2015·2015-05-27
Wright Medical Recalls Phalinx Hammertoe Handles Due to Incorrect Laser Etching
Wright Medical Technology is recalling 124 units of Phalinx Hammertoe Handles because the term DORSAL was laser etched on the incorrect side.
Product
PHALINX (TM) HAMMERTOE HANDLE, SIZE: MEDIUM, STYLE: ANGLED, REF 45304013, CONTENTS 1 EACH, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1627-2015·2015-05-27
Wright Medical Recalls PHALINX Hammertoe Handles Due to Incorrect Laser Etching
Wright Medical Technology is recalling 126 units of PHALINX Hammertoe Handles because the term 'DORSAL' was laser etched on the incorrect side.
Product
PHALINX (TM) HAMMERTOE HANDLE, SIZE: LARGE, STYLE: ANGLED, REF 45304014, CONTENTS 1 EACH, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1554-2015·2015-05-27
Philips DigitalDiagnost X-Ray System Recalled for Missing Exposure Beep Signal
Philips Medical Systems is recalling 54 DigitalDiagnost X-Ray systems because they fail to emit a beep signal after exposure if powered on for over 12 hours.
Product
Philips Healthcare DigitalDiagnost System X-Ray
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1625-2015·2015-05-27
Wright Medical Recalls Phalinx Hammertoe Handle Due to Incorrect Etching
Wright Medical Technology is recalling 121 units of Phalinx Hammertoe Handles because the word 'DORSAL' was laser-etched on the incorrect side.
Product
PHALINX (TM) HAMMERTOE HANDLE, SIZE: SMALL, STYLE: ANGLED, REF 45304012, CONTENTS 1 EACH, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1555-2015·2015-05-27
Philips DuraDiagnost X-Ray System Recalled for Missing Exposure Beep
Philips Medical Systems is recalling DuraDiagnost X-ray systems because they may fail to emit a termination beep after 12 hours of operation, violating safety regulations.
Product
Philips Healthcare DuraDiagnost X- Ray
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1624-2015·2015-05-27
Wright Medical Recalls Phalinx Hammertoe Handles Due to Incorrect Laser Etching
Wright Medical Technology is recalling 126 units of Phalinx Hammertoe Handles because the term DORSAL was laser etched on the incorrect side.
Product
PHALINX (TM) HAMMERTOE HANDLE, SIZE: X-SMALL, STYLE: ANGLED, REF 45304011, CONTENTS 1 EACH, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1083-2015·2015-05-27
Mylan Recalls Fexofenadine Hydrochloride Tablets Due to Impurity Levels
Mylan Institutional, Inc. is recalling 1,363 cartons of Fexofenadine Hydrochloride 60 mg tablets because routine stability testing showed slightly above specification results for a related compound.
Product
Fexofenadine Hydrochloride Tablets, USP 60 mg, Allergy, Non-Drowsy, Antihistamine, 100 tablets (10 X 10) per UD Cartons, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505, USA, NDC 51079-547-20
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1630-2015·2015-05-27
CooperSurgical Recalls Carter-Thomason II Port Closure System Due to Printing Defect
CooperSurgical is recalling 430 units of the Carter-Thomason II Port Closure System because pad printing on the suture guide may flake off.
Product
Carter-Thomason II Port Closure System; Model Number(s) CTI-1015P, for use in endoscopic and laparoscopic surgery.
Category
Medical Device
Distribution
Distributed nationwide