State

Nebraska product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56026–56050 of 78407

ModerateFDA (Devices)·Z-2452-2015·2015-09-02
Trilliant Surgical Recalls 3.0/4.0 Cannulated Drill Bits Due to Sizing Issue
Trilliant Surgical Ltd. is recalling 121 units of 3.0/4.0 Cannulated Drill Bits because the inner diameter is too small for the guide wire to pass through.
Product
3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw Fixation System implants are intended for fixation of fractures, non-unions, arthrodesis and osteotomies of the small bones in the hand and foot. The implants and guide…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2473-2015·2015-09-02
Baxter MiniCap Extended Life PD Transfer Set Labeling Recall
Baxter Healthcare Corp. is recalling 33,474 units of MiniCap Extended Life PD Transfer Sets to update labeling with additional safety instructions and warnings.
Product
MiniCap Extended Life PD Transfer Set. Product Code 5C4449. intended for use with Baxter Locking titanium adapter for peritoneal dialysis catheter in disconnect applications and in cycler applications where aseptic connections and disconnections are performed at the transfer…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1373-2015·2015-09-02
Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets
Dr. Reddy's Laboratories is recalling 1,056 bottles of Amlodipine Besylate and Atorvastatin Calcium tablets because the atorvastatin component is subpotent.
Product
AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2468-2015·2015-09-02
Stryker recalls mislabeled 5mm trocar sleeves due to length discrepancy
Stryker Sustainability Solutions is recalling 90 reprocessed trocar sleeves labeled as 100mm but containing 75mm models.
Product
Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery, Inc. Excel Trocar Sleeve w/Stability Sleeve 5mm x 100mm Reprocessed by Stryker Sustainability Solutions Product Usage: The Reprocessed Ethicon ENDOPATH¿ XCEL Universal Trocar Stability Sleeve is a sterile…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2448-2015·2015-09-02
Alcon Recalls LX3 Microscope Floor Stands Due to Cabling Issues
Alcon is voluntarily recalling LX3 Microscope Floor Stands because cabling issues may cause loss of functionality or illumination failure.
Product
LX3 Floor Stand for Endure Luxite Envision Optical System; Endure LuxOR Q-Vue. Product Usage: The LX3 Microscope Floor Stand is an accessory to the LuxOR Opthalmic Microscope and the LuxOR Opthalmic Microscope with Q-VUE 3-D Assistant Visualization and provides a portable…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2471-2015·2015-09-02
Baxter Recalls MiniCap Peritoneal Dialysis Transfer Sets for Labeling Updates
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets to update labeling with new safety instructions and warnings.
Product
MiniCap Extended Life PD Transfer Set Extra Short (4") with Twist Clamp. Product Code: 5C4483. intended for use with Baxter Locking titanium adapter for peritoneal dialysis catheter in disconnect applications and in cycler applications where aseptic connections and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1369-2015·2015-09-02
Mucinex Fast-Max DM Max Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast-Max DM Max bottles because the back label is missing active ingredients and safety warnings.
Product
MUCINEX FAST-MAX DM MAX AND MUCINEX NIGHTTIME COLD AND FLU — MUCINEX FAST-MAX DM MAX AND MUCINEX NIGHTTIME COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND TRIPROLIDINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1370-2015·2015-09-02
Taro Recalls Topicort Topical Spray Due to Impurity Test Failures
Taro Pharmaceuticals is recalling Topicort topical spray because impurity testing failed at 6 and 9 months. The recall covers 16,320 bottles distributed nationwide.
Product
TOPICORT — TOPICORT (DESOXIMETASONE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1376-2015·2015-09-02
Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets
Dr. Reddy's Laboratories is recalling specific lots of Amlodipine Besylate and Atorvastatin Calcium tablets because they contain subpotent atorvastatin.
Product
AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1374-2015·2015-09-02
Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets
Dr. Reddy's Laboratories is recalling 576 bottles of Amlodipine Besylate and Atorvastatin Calcium tablets because the atorvastatin component is subpotent.
Product
AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1375-2015·2015-09-02
Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets
Dr. Reddy's Laboratories is recalling 984 bottles of Amlodipine Besylate and Atorvastatin Calcium tablets because the atorvastatin component is subpotent.
Product
AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1379-2015·2015-09-02
Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets
Dr. Reddy's is recalling Amlodipine Besylate and Atorvastatin Calcium tablets because the atorvastatin component was found to be subpotent.
Product
AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1371-2015·2015-09-02
KVK-Tech Recalls Phentermine Hydrochloride Capsules Due to Impurity Failures
KVK-Tech is recalling specific lots of Phentermine Hydrochloride Capsules because they failed impurity specifications during stability testing.
Product
Phentermine Hydrochloride Capsules, USP, 15 mg, packaged in a) 100-count bottle (NDC 10702-0026-01; UPC 3 10702 02601 8) and b) 1000-count bottle (NDC 10702-0026-10; UPC 3 10702 02601 0); Rx only, Mfd. by KVK-TECH, Inc., Newtown, PA
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1378-2015·2015-09-02
Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets
Dr. Reddy's is recalling specific lots of Amlodipine Besylate and Atorvastatin Calcium tablets because they contain subpotent atorvastatin.
Product
AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15E071000·2015-09-01
Specialty Products Company Recalls Aftermarket Suspension Alignment Hardware Kits
Specialty Products Company is recalling aftermarket alignment hardware kits for certain Mercedes-Benz and Chrysler/Dodge vehicles because the suspension bolts may fracture, potentially causing loss of vehicle control.
Product
SUSPENSION recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V548000·2015-09-01
Spartan Recalls 2007-2008 Motorhome Chassis Due to Wheel Bearing Fire Risk
Spartan Motors is recalling 440 motorhome chassis because tight wheel bearings may overheat and cause a fire.
Product
SPARTAN — SPARTAN K2, MM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V549000·2015-09-01
Spartan Motorhomes Recalled for Potential Engine Cooling Fan Separation
Spartan Motors USA is recalling 2004-2008 K2, K3, and MM motorhomes because the engine cooling fan may separate from the drive, posing an injury risk to nearby individuals.
Product
SPARTAN — SPARTAN MM, K3, K2
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·15228·2015-09-01
MiWorld Recalls iPhone Wall Chargers Due to Fire Hazard
MiWorld Accessories is recalling iPhone 5/5S wall chargers sold at Charlotte Russe because they can overheat and catch fire. One fire incident was reported.
Product
USB Cord & Wall Chargers for iPhone 5/5S
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·15V550000·2015-09-01
Kawasaki Recalls Vulcan 1700 Motorcycles for Ignition Wire Chafing Risk
Kawasaki is recalling specific Vulcan 1700 Voyager and Vaquero motorcycles because an ignition wire may chafe against the fuel tank, causing a short circuit and potential engine stall.
Product
KAWASAKI — KAWASAKI VULCAN 1700 VOYAGER, VULCAN 1700 VAQUERO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V547000·2015-09-01
Spartan Gladiator and MetroStar Emergency Vehicles Recalled for Mirror Defect
Spartan Motors is recalling 2008-2010 Gladiator and MetroStar emergency vehicles because mirror lenses may fall off due to vibration, impairing driver visibility.
Product
SPARTAN — SPARTAN GLADIATOR, METROSTAR
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·117-2015·2015-08-31
Ocho Rios Recalls Canned Corned Beef Lacking Import Inspection
Ocho Rios is recalling approximately 7,228 pounds of canned corned beef imported from Brazil that was not presented for U.S. inspection. No adverse reactions have been reported.
Product
Ocho Rios Recalls Corned Beef Products Produced Without Benefit of Import Inspection
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·15V545000·2015-08-31
Micro Bird Recalls 2013-2015 G5 School Buses for Battery Fire Risk
Micro Bird is recalling 283 G5 school buses due to corroding battery studs that may cause fires or component damage.
Product
MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V546000·2015-08-31
Mitsubishi Recalls Lancer Models Due to Fuel Tank Fire Risk
Mitsubishi is recalling 2014-2015 Lancer Evolution and Ralliart vehicles because a parking brake cable may wear the fuel tank coating, increasing fire risk.
Product
MITSUBISHI — MITSUBISHI LANCER EVOLUTION, LANCER RALLIART
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V544000·2015-08-31
Micro Bird Recalls 2013-2015 G5 Transit Buses for Battery Fire Risk
Micro Bird is recalling 2013-2015 G5 transit buses because corroded battery studs may cause short circuits and fires, or missing bolts may cause battery detachment.
Product
MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
LowUSDA FSIS·118-2015·2015-08-31
Holten Meat Recalls Beef Patties Due to Unlabeled MSG
Holten Meat Inc. is recalling approximately 501,509 pounds of Extra Value Meats Quarter Pound Beef Patties because monosodium glutamate (MSG) was used but not listed on the label.
Product
Branding Iron Holdings - Holten Meat — Recall Notification Report 118-2015 (Beef Patties)
Category
Food
Distribution
Distributed nationwide