State

Nebraska product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3626–3650 of 78317

SevereFDA (Devices)·Z-1547-2026·2026-03-18
TRUE METRIX AIR manuals recalled as Class I over E-5 guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX AIR blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX AIR Kit/REA4001-01, Leader TRUE METRIX AIR Kit/REA4002-01, CVS TRUE METRIX AIR Kit/REA4007-01, GNP TRUE METRIX AIR…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0548-2026·2026-03-18
Vegetarian Chicken Flavor Ramen Express contains undeclared Yellow #5
Palmetto Gourmet Foods Inc. is recalling Vegetarian Chicken Flavor Ramen Express because the product contains undeclared Yellow #5 food coloring, a major allergen for some consumers.
Product
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***) Palm oil***" Contains: Wheat, Soy. UPC 8 10037 81004 2 Produced by PALMETTO GOURMET FOODS, INC SALUDA, SC 29138
Category
Food
Distribution
32 states
HighFDA (Devices)·Z-1523-2026·2026-03-18
Link Endo-Model plateau 15-0027/16 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/16 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/16;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1528-2026·2026-03-18
GEM Premier 5000 PAK part 00055407504 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407504 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055407504.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1520-2026·2026-03-18
Link Endo-Model plateau 15-8521/15 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/15 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8521/15;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1532-2026·2026-03-18
GEM Premier 5000 PAK part 00055415004 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055415004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055415004.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1512-2026·2026-03-18
Link Endo-Model plateau 15-0027/15 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/15 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/15;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V161000·2026-03-18
2026 Keystone Montana Fifth Wheel Recreational Trailers Electrical Wiring Recall
Keystone is recalling certain 2026 Montana fifth wheel trailers because improperly secured 12-volt and 120-volt wiring may be pinched and damaged when the bedroom slide-out moves, increasing fire risk.
Product
KEYSTONE — KEYSTONE MONTANA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1497-2026·2026-03-18
IBA proton therapy system may not interrupt beam when gating fails
Ion Beam Applications is recalling PROTEUS 235 proton therapy systems because a disabled interface means the safety system may not interrupt beam delivery if the external gating signal is lost.
Product
IBA Proton Therapy System - PROTEUS 235
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1522-2026·2026-03-18
Link Endo-Model plateau 15-0027/12 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/12;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1554-2026·2026-03-18
Artelon FlexBand Dynamic Matrix failed bacterial endotoxin testing
International Life Sciences is recalling the Artelon FlexBand Dynamic Matrix, ref 31057, because the augmentation devices failed bacterial endotoxin testing.
Product
Artelon FlexBand Dynamic Matrix Ref: 31057
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2026·2026-03-18
Link Endo-Model plateau 15-2836/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-2836/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-2836/11;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1552-2026·2026-03-18
Beckman Coulter DxC 700 AU analyzer may stop analyzing after errors
Beckman Coulter is recalling DxC 700 AU analyzers because leaving the calibration monitor open beyond 15 minutes can trigger database errors that stop the system analyzing.
Product
DxC 700 AU, REF: B86444, B86446
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1511-2026·2026-03-18
Link Endo-Model SL component 16-2840/05 recalled over bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/05 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1525-2026·2026-03-18
GEM Premier 5000 PAK part 00055360008 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055360008.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1534-2026·2026-03-18
GEM Premier 5000 part 00055415008 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055415008.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1535-2026·2026-03-18
GEM Premier 5000 part 00055415010 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415010 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055415010.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1555-2026·2026-03-18
Artelon FlexBand Plus implants failed bacterial endotoxin testing
International Life Sciences is recalling Artelon FlexBand Plus, refs 41054 and 41057, because the augmentation devices failed bacterial endotoxin testing.
Product
Artelon FlexBand Plus Ref: 41054 & 41057
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2026·2026-03-18
Link Endo-Model SL component 16-2840/02 recalled over bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/02 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1531-2026·2026-03-18
GEM Premier 5000 PAK part 00055407511 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407511 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055407511.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1540-2026·2026-03-18
GEM Premier 5000 part 00055430011 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055430011.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V165000·2026-03-18
Ford and Lincoln image module resets can disable rearview camera
Ford is recalling certain 2022-2025 Lincoln Navigator, Nautilus, Aviator and Explorer vehicles because the Image Processing Module A may reset unexpectedly, losing the rearview camera image and driver assistance features.
Product
LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER, NAUTILUS, NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1529-2026·2026-03-18
GEM Premier 5000 PAK part 00055407508 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407508 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055407508.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1544-2026·2026-03-18
Infant and child defibrillator electrodes recalled over pediatric electrode delamination
Physio-Control is recalling Infant/Child Reduced Energy Defibrillator Electrodes, catalogue numbers 11101-000016 and 11101-000017, due to pediatric defibrillator electrode delamination.
Product
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalog Number: 11101-000017 UDI-DI code: 00721902682483 Infant/Child Reduced Energy Defibrillation Electrodes are pre gelled, self-adhesive…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1563-2026·2026-03-18
Medline Medcrest surgical gowns may delaminate prematurely after recommended laundering
Medline is recalling Medcrest surgical gowns because the fabric may delaminate prematurely when the included laundering instructions are followed.
Product
Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4JXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XL MDTGXC4JXXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XX MDTGXP4JL…
Category
Medical Device
Distribution
Distributed nationwide