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.

56001–56025 of 78407

HighFDA (Devices)·Z-2443-2015·2015-09-02
Recall of Infant Heel Warmers Due to Potential Breakage and Spillage
The FDA is recalling 68,800 units of Infant Heel Warmers because they may break during activation, causing spillage of contents that could irritate skin or eyes.
Product
Covidien Argyle Infant Heel Warmers (no tab) Item Code: MH00002N Product Usage: Intended for application of the right amount of heat to an infants heel for blood sampling
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2444-2015·2015-09-02
FDA Recalls Covidien Infant Heel Warmers Due to Breakage Risk
The FDA is recalling 164,749 units of Covidien Infant Heel Warmers because they may break during activation, causing spillage and potential skin or eye irritation.
Product
Covidien Argyle Infant Heel Warmers (with tab) Item Code: MH00002T Product Usage: Intended for application of the right amount of heat to an infants heel for blood sampling.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-3049-2015·2015-09-02
Veggie Evolution Kale Crisps Recalled for Undeclared Milk Allergen
It Takes A Village Foods is recalling Veggie Evolution Kale Crisps Lemon Parmesan because the label lists Parmesan cheese but fails to declare milk as an allergen.
Product
Kale Crisps Lemon Parmesan sold under brand Veggie Evolution, each plastic package has a net weight 1.5 oz. There are six packages per case. UPC is 7 94504 69431 4. The product's label is read in part: "***VEGGIE EVOLUTION***KALE CRISPS***LEMON PARMESAN***INGREDIENTS: KALE…
Category
Food
Distribution
22 states
HighFDA (Devices)·Z-2467-2015·2015-09-02
Sunrise Medical Recalls Quickie IRIS Wheelchairs with Dynamic Backrest
Sunrise Medical is recalling 64 Quickie IRIS wheelchairs because the backrest system may break, posing a risk of falls or injury to the occupant.
Product
Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code 183M02 - MONO Backrest system with Dynamic Backrest option. Provide mobility to persons limited to a sitting position.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·15230·2015-09-02
Tadpoles Moses Basket and Stand Recalled for Fall Hazard
Sleeping Partners is recalling Tadpoles Moses baskets and stands because the basket can slide off inclined surfaces and the stand can tip, posing a fall hazard to infants.
Product
Tadpoles Baby and Kids Moses Basket and Stand
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-3050-2015·2015-09-02
Veggie Evolution Vegetable Crisps Recalled for Undeclared Milk Allergen
It Takes A Village Foods, LLC is recalling Vegetable Crisps Lemon Parmesan because the label declares Parmesan cheese but fails to declare milk as an allergen.
Product
Vegetable Crisps Lemon Parmesan sold under brand Veggie Evolution, each poly pouch has a net weight 2 oz. There are 6 packages per case. UPC is 7 36211 15015 8. The product's label is read in part: "***VEGGIE EVOLUTION***VEGETABLE CRISPS***LEMON PARMESAN***INGREDIENTS…
Category
Food
Distribution
22 states
HighCPSC·15229·2015-09-02
Imagine Nation Books Recalls Pink Giraffe Animal Purse for Lead Paint
Imagine Nation Books is recalling Pink Giraffe Animal Purses because the red zipper paint contains excessive lead, violating federal standards.
Product
Pink Giraffe Animal Purse
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·15V553000·2015-09-02
Forest River Recalls 2016 Shasta Airflyte Trailers Due to Window Defect
Forest River is recalling 2016 Shasta Airflyte 16 and 19 trailers because rear exit window glass may detach and fall onto the road.
Product
SHASTA — SHASTA AIRFLYTE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2466-2015·2015-09-02
Sunrise Medical Recalls Quickie and Zippie IRIS Wheelchairs with MONO Backrest
Sunrise Medical is recalling 64 Quickie and Zippie IRIS wheelchairs because the MONO Backrest System may break, posing a risk of falls or injury to the occupant.
Product
Zippie IRIS Wheelchair. model EIZ5A in combination with option code 188M02 - MONO Backrest system with Dynamic Backrest option. Provide mobility to persons limited to a sitting position.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2445-2015·2015-09-02
FDA Recalls Omnilife Apex Interface Acetabular Shells Due to Design Defect
Omnilife Science Inc. is recalling 112 Apex Interface Hemi 54X and Flared 56X acetabular shells because improper screw hole placement may occur due to inaccurate index line location.
Product
APEX INTERFACE Hemi 54X and Flared 56X, 3 Hole Acetabular Shells; Model: H5-12354, H5-11356. Product Usage: The Apex Interface Acetabular System is intended for use in combination with the Apex Modular Hip Stem in total hip replacement procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V555000·2015-09-02
Volvo Recalls 2016 Models Due to Starter Motor Fuse Failure Risk
Volvo is recalling 7,855 model year 2016 vehicles because a starter motor fuse may blow, preventing the car from restarting in traffic and increasing crash risk.
Product
VOLVO — VOLVO S60, V60, XC60, XC70
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2450-2015·2015-09-02
Siemens Recalls Dimension Vista B2-Microglobulin Reagent Cartridges
Siemens Healthcare Diagnostics is recalling 1,655 Dimension Vista B2-Microglobulin Flex Reagent Cartridges due to potential reagent contamination that may cause falsely low test results.
Product
Dimension Vista B¿2-Microglobulin Flex Reagent Cartridge (B2MIC); Product Usage: The B2MIC method is an in vitro diagnostic test for the quantitative measurement of B¿2-Microglobulin in human serum, heparinized plasma, EDTA plasma and urine on the Dimension Vista System.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2383-2015·2015-09-02
Philips DigitalDiagnost X-ray Systems Recalled for Missing Exposure Beep Signal
Philips is recalling 62 DigitalDiagnost X-ray systems because a software defect prevents the exposure termination beep from sounding after 12 hours of operation.
Product
Philips DigitalDiagnost Release 4.0.3, Release 4.1/4.1.1. excluding systems with SP1 Product Usage: The DigitalDiagnost is intended for use in generating radiographic images of human anatomy by qualified/trained doctors or technicians.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15E072000·2015-09-02
Peter Paul Nitrous Oxide Solenoid Valve Recall for Potential Breakage
Peter Paul Electronics is recalling specific nitrous oxide solenoid valves because end stops may break under pressure, posing an injury risk to nearby individuals.
Product
FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2472-2015·2015-09-02
Baxter MiniCap Peritoneal Dialysis Transfer Set Labeling Recall
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets to update labeling with safety instructions and warnings.
Product
MiniCap Extended Life PD Transfer Set (6") with Twist Clamp. Product Code: 5C4482. 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…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-3054-2015·2015-09-02
Nepali Finger Chips Recalled for Undeclared Tartrazine
Balajee Trade Link LLC is recalling Rato Bhale Nepali Finger Chips because the product contains undeclared tartrazine (yellow #5).
Product
Rato Bhale Nepali Finger Chips Product of Nepal Weight: 200g (7.05 OZ) Imported by: Balajee Trade Link, LLC, PA USA Batch No. 01-15
Category
Food
Distribution
9 states
ModerateFDA (Drugs)·D-1377-2015·2015-09-02
Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets
Dr. Reddy's Laboratories is recalling 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-2477-2015·2015-09-02
Nidek OPD-Scan III Recall for Software Aberration Calculation Error
Nidek Inc is recalling 3,836 OPD-Scan III Refractive Power/Corneal Analyzers due to a software bug that incorrectly calculates high-order aberrations.
Product
OPD-Scan III Refractive Power/Corneal Analyzer Opthalmic Software versions 1.00.08 1.05.07 1.10.01, 1.01.02 1.06.02 1.11.02, 1.02.01 1.07.01 1.12.03, 1.03.02 1.08.01 1.13.01, 1.04.03 1.09.01. Opthalmic: The OPD-Scan III is a diagnostic instrument that is indicated for use…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2441-2015·2015-09-02
Iris Diagnostics Recalls iChemVELOCITY Urine Chemistry Systems for Labeling Error
Iris Diagnostics is recalling iChemVELOCITY Automated Urine Chemistry systems because they do not maintain the claimed 5-day strip stability under specified conditions.
Product
iChemVELOCITY Automated Urine Chemistry Catalog No. 800-3049, 800-3050, 800-3079, 800-3080, 800-3530, 800-7167, 800-7190, 800-7713,800-7714, 800-7719, 800-7720. An in vitro diagnostic device used to automate the urine chemistry analysis profile using iChemVELOCITY Urine…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2475-2015·2015-09-02
Synthes Sternal ZIPFIX Application Instrument Recalled Due to Detaching End Cap
Synthes (USA) Products LLC is recalling 451 Sternal ZIPFIX Application Instruments because the end cap may loosen and detach, rendering the instrument non-functional.
Product
Synthes Application Instrument for Sternal ZIPFIX; indications for use include primary or secondary closure/repair of the sternum following sternotomy or fracture of the sternum to stabilize the sternum and promote fusion
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2469-2015·2015-09-02
GE Healthcare Recalls Centricity PACS-IW Systems Due to Missing Images
GE Healthcare is recalling 82 Centricity PACS-IW systems because medical images may be missing when a specific system parameter is set to a value greater than 1.
Product
Centricity PACS-IW with Universal Viewer Product Usage: The Centricity PACS-IW with Universal Viewer is a picture archiving and communications system, a device that provides one or more capabilities relating to the acceptance, transfer, display, storage, and digital…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2459-2015·2015-09-02
Advanced Sterilization Products Recalls CIDEX Activated Dialdehyde Solution
Advanced Sterilization Products is recalling CIDEX Activated Dialdehyde Solution because it may lack adequate data to support its 24-month shelf life.
Product
CIDEX Activated Dialdehyde Solution, 4 bottles/case, P/N: 2266
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2474-2015·2015-09-02
Baxter Recalls CAPD Solution Transfer Sets for Labeling Revisions
Baxter Healthcare Corp. is recalling 35,460 units of CAPD Solution Transfer Sets to update labeling with additional safety instructions and warnings.
Product
CAPD Solution Transfer Set with Locking Connector. Product Code: 5C4160. intended for use with containers of DIANEAL peritoneal dialysis solution.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2449-2015·2015-09-02
Carestream DRX-Evolution X-Ray System Recalled for Image Stitching Defect
Carestream Health is recalling DRX-Evolution X-ray systems due to a software defect that may cause undetected image stitching inconsistencies.
Product
CARESTREAM DRX-EVOLUTION X-Ray System Product Usage: The device is a permanently installed diagnostic X-ray system for general radiographic x-ray imaging including tomography. The tomography feature is not to be used for imaging pediatric patients.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2464-2015·2015-09-02
Trilliant Surgical Recalls Tiger Cannulated Screw System Tray Lids
Trilliant Surgical Ltd. is recalling 71 units of Tiger Cannulated Tray Lids because they are occasionally difficult to remove from sterilization trays.
Product
Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE; Combined Tiger/Headless Screw Part # 210-99-101 NON-STERILE; These are components of the Tiger Cannulated Screw System and the Tiger Headless Cannulated Screw System The Tiger Cannulated Screw Fixation System and the…
Category
Medical Device
Distribution
Distributed nationwide