State

Nebraska product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52526–52550 of 78404

HighFDA (Devices)·Z-1395-2016·2016-04-20
C.R. Bard Recalls ArcticGel Pads Due to Flow Rate Issues
C.R. Bard is recalling 21,412 ArcticGel Pads used with the Arctic Sun Temperature Management System because of complaints regarding restricted or inaccurate flow rates.
Product
BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management System is intended for monitoring and controlling patient temperature. ArcticGel Pads are only for use with an Arctic Sun Temperature Management System Control Module.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1369-2016·2016-04-20
ICU Medical Recalls Diana Automated Compounding System Due to Accuracy Issues
ICU Medical is recalling 49 units of the Diana Automated Compounding System because it may not meet accuracy specifications when mixing volumes under 5ml.
Product
Diana Automated Compounding System, Diana V1.3, Item No. CH5300, CH5300R The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0824-2016·2016-04-20
Morrison Milling Recalls HEB Fish Fry Mix Due to Metal Fragments
Morrison Milling is recalling HEB Original Seasonal Fish Fry Mix because it may contain small metal fragments from a wire mesh sifter.
Product
HEB Original Seasonal Fish Fry Mix NET WT. 16 OZ (1 LB) CONT. NET 454g and HEB Original Seasonal Fish Fry Mix NET WT. 10 OZ CONT. NET 284g packed in paper box
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1387-2016·2016-04-20
Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks
Synthes (USA) Products LLC is recalling 317 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if removal is attempted.
Product
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16149·2016-04-20
YTL International Recalls Drywall Lifts Due to Injury Hazard
YTL International is recalling about 17,000 drywall lifts because they can fail and drop loads, posing an injury risk. No injuries have been reported.
Product
Drywall lifts
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1388-2016·2016-04-20
Arjo Concerto Basic Shower Trolley Recalled for Loose Bolts
Arjo is recalling 1,596 Concerto Basic Shower Trolleys because bolts connecting the stretcher to the hydraulic piston and tilting mechanism may become loose.
Product
The Concerto Basic Shower Trolley is intended for assisted hygiene care, especially showering and bathing of residents in care environments such as senior/assisted living, group home, special care, nursing homes, hospitals and home care. The Concerto Basic Shower Trolley is…
Category
Medical Device
Distribution
36 states
HighFDA (Food)·F-1074-2016·2016-04-20
Hidden Valley Original Ranch Dressing Recalled for Missing Soy Label
The Clorox Company is recalling Hidden Valley Original Ranch dressing because some bottles are missing the soy lecithin ingredient declaration.
Product
Hidden Valley Original Ranch dressing, 16 fl oz. ( 473 ml). plastic bottles; Ingredients: Vegetable oil (soybean and/or Canola oil) water, egg yolk, sugar, Salt, Cultured non fat buttermilk, natural flavors (milk, soy), less than 1% spiced, dried garlic, dried onion, vinegar…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1380-2016·2016-04-20
Philips EPIQ Ultrasound Systems Recalled for Control Panel Fastener Loosening
Philips is recalling EPIQ diagnostic ultrasound systems because fasteners securing the control panel may loosen, potentially causing the assembly to detach.
Product
EPIQ DIAGNOSTIC ULTRASOUND SYSTEM, Model EPIQ 5C, EPIC 5G, EPIQ 5W, EPIQ 7C, EPIC 7GC, and EPIQ 7W. Diagnostic Ultrasound System for ultrasound imaging in abdominal, cardiac adult, cardiac other (fetal), cardiac pediatric, cerebral vascular, cephalic (adult), cephalic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1373-2016·2016-04-20
Maquet Rotaflow Centrifugal Pump Tubing Recalled for Endotoxin Risk
Maquet Cardiovascular is voluntarily recalling Rotaflow Centrifugal Pump custom tubing packs due to a potential risk of endotoxin exposure.
Product
Rotaflow Centrifugal Pump Custom tubing packs for the oxygenator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1376-2016·2016-04-20
Intuitive Surgical Recalls da Vinci S Surgical System User Manuals
Intuitive Surgical is recalling da Vinci S Surgical System user manuals because using certain instruments with ablation probes can increase microscopic metallic particulates.
Product
da Vinci S Surgical System (IS1200/IS2000/IS3000) user manual, instrument & accessory. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments including rigid…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0864-2016·2016-04-20
Marie Callender's Corn Bread Mix Recalled for Metal Fragments
Morrison Milling is recalling Marie Callender's Low Fat Southwestern Corn Bread Mix because it may contain small metal fragments from a wire mesh sifter.
Product
Marie Callender's Low Fat Southwestern Corn Bread Mix NET WT 1 lb (16 oz. ) 454 grams
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1356-2016·2016-04-20
Philips Ingenuity CT Systems Recalled for Software Error in Data Transmission
Philips Medical Systems is recalling 82 Ingenuity CT systems due to a software error that may prevent the automatic transmission of image data to remote devices.
Product
Ingenuity CT Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes
Category
Medical Device
Distribution
43 states
ModerateFDA (Devices)·Z-1365-2016·2016-04-20
ICU Medical Recalls Diana Automated Compounding Systems for Accuracy Issues
ICU Medical is recalling 57 Diana Automated Compounding Systems because they may not accurately mix volumes under 5ml.
Product
Diana Automated Compounding System, Diana Onco Plus 1.2, Item No. ASN222, ASN222-GST, ASN222-R The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0880-2016·2016-04-20
Pioneer Buttermilk Pancake Mix Recalled for Potential Metal Fragments
Morrison Milling is recalling Pioneer Original Buttermilk Pancake & Waffle Mix because it may contain small metal fragments from a wire mesh sifter.
Product
Pioneer Original Buttermilk Pancake & Waffle Mix NET WT 5 LBS 2.27 kg and Pioneer Original Buttermilk Pancake & Waffle Mix NET WT 25 LBS 11.34 kg
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1045-2016·2016-04-20
L'Bri Aloe Health Juice Drink Recalled for Unlabeled Sodium Metabisulfite
Cosmetic Labs LP is recalling L'Bri Pure N' Natural Nutri Aloe Health Juice Drink because it contains sodium metabisulfite, an ingredient not listed on the label.
Product
L'Bri Pure N' Natural Nutri Aloe Health Juice Drink 960 mL 32 FL. OZ. and L'Bri Pure N' Natural Nutri Aloe Health Juice Drink 1 FL OZ./29 mL
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0877-2016·2016-04-20
Conestoga Buttermilk Pancake Mix Recalled for Metal Fragment Risk
Morrison Milling is recalling Conestoga Buttermilk Pancake Mix because it may contain small metal fragments from a wire mesh sifter.
Product
Conestoga Buttermilk Pancake Mix NET WT. 5 LB. (2.27 kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1391-2016·2016-04-20
X-NAV Recalls X-Guide Surgical Navigation System X-Clip Bulk Kits
X-NAV Technologies is recalling 845 X-Guide Surgical Navigation System X-Clip Bulk Kits because the stainless steel fiducials may not meet specifications.
Product
X-Guide Surgical Navigation System, X-Clip Bulk Kit The X-Guide Surgical Navigation System is a computerized navigational system intended to provide assistance in both the preoperative planning phase and the intra-operative surgical phase of dental implantation procedures.
Category
Medical Device
Distribution
14 states
ModerateFDA (Food)·F-0891-2016·2016-04-20
Morrison Milling Recalls Multigrain Pancake Mix Due to Metal Fragments
Morrison Milling is recalling American Blue Ribbon Multigrain Pancake Mix because it may contain small metal fragments from a wire mesh sifter.
Product
American Blue Ribbon Holdings. LLC Multigrain Pancake Mix NET WT 37.5 LBS (17.01 kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1379-2016·2016-04-20
Stryker SurgiCounter Scanner Recalled for Software Interaction Errors
Stryker is recalling 286 SurgiCounter scanners because they may display error messages and fail to display software version numbers correctly in the SC360 application.
Product
SurgiCounter scanner, part of the SurgiCount Safety-Sponge System. Model numbers 0694-097-000 and 0694-097-001. Product Usage: The SurgiCount Safety Sponge System is indicated for use in counting and recording the number of thermally labeled surgical sponges, laparotomy…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0858-2016·2016-04-20
Hartz Krispy Chicken 'N' Rolls Milk Dip Recalled for Metal Fragments
Morrison Milling is recalling Hartz Krispy Chicken 'N' Rolls Milk Dip because it may contain small metal fragments from a wire mesh sifter.
Product
Hartz Krispy Chicken 'N' Rolls Milk Dip Net Wt 20 LBS (9.07 kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0868-2016·2016-04-20
Morrison's Corn Bread Mix Recalled for Potential Metal Fragments
Morrison's Country Style Corn Bread Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.
Product
Morrison's Country Style Corn Bread Mix NET WT 25 LB (11.33 kg) and Morrison's Country Style Cornbread Mix NET WT 5 LB (2.27 kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0873-2016·2016-04-20
Fletcher's Corny Dog Mix Recalled for Potential Metal Fragments
Morrison Milling is recalling Fletcher's Corny Dog Mix because it may contain small metal fragments from a wire mesh sifter.
Product
Fletcher's Corny Dog Mix NET WT 25 LB (11.33 kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0849-2016·2016-04-20
Champs Chicken Batter Mix Recalled for Potential Metal Fragments
Morrison Milling is recalling Champs Chicken Batter Mix because it may contain small metal fragments from a wire mesh sifter.
Product
Champs Chicken Batter Mix Net Wt. 25 lbs. (11.33 Kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0860-2016·2016-04-20
Morrison Milling Recalls On The Border Tempura Batter Due to Metal Fragments
Morrison Milling is recalling On The Border Tempura Batter because it may contain small metal fragments from a wire mesh sifter.
Product
On The Border Mexican Grill & Cantina Tempura Batter Net Wt 25 LBS (11.34 kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1357-2016·2016-04-20
Bard Foley Catheter Recalled for Incorrect Inflation Volume Labeling
C.R. Bard is recalling 1.4 million Bardex Foley catheters because the instructions for use list an incorrect inflation volume.
Product
BARDEX I.C. Anti-Infective 2-Way 3cc Foley Catheter, Rx only. Intended for urinary bladder drainage in female patients requiring catheterization for management of incontinence, voiding dysfunction and surgical procedure.
Category
Medical Device
Distribution
Distributed nationwide