State

Nebraska product recalls

73,092 recalls have nationwide distribution and so reach Nebraska. 4,575 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total: 4,575
Critical: 715
Severe: 1,131
Most recent: 2026-09-23

Of the 4,575 recalls naming Nebraska we have scored against our rubric, 715 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,131 (25%) are Severe.

Which agencies issued them

These figures cover only the 4,575 recalls whose distribution notice names Nebraska specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9951–9975 of 77667

HighFDA (Devices)·Z-3174-2024·2024-09-25
Hemodialysis tubing may fail to flow if connector is incompletely inserted
B Braun's STREAMLINE FRESENIUS bloodline tubing used in hemodialysis may have a design issue where incomplete insertion of the patient connector prevents proper blood flow during certain procedures. Patients receiving dialysis may experience treatment delays.
Product
STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3146-2024·2024-09-25
Medical imaging systems vulnerable to unauthorized access due to software vulnerability
GE Healthcare ViewPoint 6 medical imaging systems contain a software vulnerability (CVE-2023-43208) in Mirth Connect that could allow unauthorized access and patient data manipulation. 574 units are affected and distributed nationwide.
Product
ViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA, c) H47591MT, d) H47591PE, e) H47591PR, f) H47591RA, g) H47591SD, h) H47591YA; system, imaging processing, radiological
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3159-2024·2024-09-25
Convenience kits recalled for containing defective medical syringes
ROi CPS LLC is recalling medical convenience kits distributed with Merit syringes that were subsequently recalled by their manufacturer. Approximately 3,387 kits with multiple lot numbers were affected.
Product
regard Clinical Packaging Solutions, HT00376I - SPECIAL PROCEDURE, Item Number 800223009
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3168-2024·2024-09-25
Philips MultiDiagnost Eleva X-ray system cable hose carrier detachment
Philips is recalling 109 MultiDiagnost Eleva X-ray systems worldwide due to potential cable hose carrier detachment from broken plastic or bolts, which could cause parts to fall and result in injury.
Product
System Name: 708038 MultiDiagnost Eleva with Flat Detector 708037 MultiDiagnost Eleva with Flat Detector 708036 MultiDiagnost Eleva 708034 MultiDiagnost Eleva with Flat Detector 708032 MultiDiagnost Eleva
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3138-2024·2024-09-25
Infusion Pump Alaris System PC Unit 8015 Recalled for Bent Connector
CareFusion's Alaris System PC Unit Model 8015 infusion pumps are being recalled due to a bent female IUI connector affecting over 125,000 devices. The defect may prevent the device from operating properly or delay infusion or monitoring startup.
Product
Alaris System PC Unit Model 8015 - a modular infusion pump and monitoring system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3166-2024·2024-09-25
Philips Allura Xper Fluoroscopy Systems Cable Hose Carrier Detachment
Philips Allura Xper FD series fluoroscopy systems may have detached cable hose carriers due to broken plastic or bolts. A detachment could cause parts to fall and potentially result in injury.
Product
System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Xper FD20/15 722039 Allura Xper FD20/20 OR Table 722038 Allura Xper FD20/20 722035 Allura Xper FD20 OR Table 722029 Allura Xper FD20/10 722028 Allura Xper FD20 722027 Allura Xper FD10/10 722026 Allura Xper FD10 722025
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3178-2024·2024-09-25
Streamline Bloodline Hemodialysis Sets Recalled for Patient Connector Defect
B. Braun is recalling 9,864,165 Streamline Bloodline Sets nationwide due to incomplete patient connector insertion. The defect may restrict fluid flow during hemodialysis and cause therapy delays.
Product
STREAMLINE BLOODLINE SET FOR DIALOG-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2010M2096
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3140-2024·2024-09-25
Alaris EtCO2 Module Model 8300 Recalled Due to Bent Connector
CareFusion 303, Inc. recalls 180 Alaris EtCO2 Module Model 8300 units with potentially bent female connectors that may prevent device operation, risking delays in infusion and monitoring.
Product
Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3173-2024·2024-09-25
Hemodialysis Bloodline Tubing Recall Over Incomplete Connector Insertion Risk
B Braun is recalling SL BLOODLINE FOR FMC 2008 SERIES hemodialysis tubing nationwide due to incomplete connector insertion that may cause blood flow restrictions during treatment.
Product
SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3180-2024·2024-09-25
Beckman Coulter Analyzer Recalled for Pneumatic Tubing Defects
Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to undersized pneumatic tubing in the reagent storage module, which can cause air leaks and compressor failures, potentially leading to test errors and delayed results.
Product
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Model Number C21510, RSM Pneumatic Tubing Kit item #2, REF C11137; in vitro diagnostic instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3179-2024·2024-09-25
B Braun Streamline Bloodline Set Recalled for Potential Occlusion
B Braun Medical Inc. is recalling Streamline Bloodline Sets because incomplete connector insertion may cause flow restrictions during hemodialysis.
Product
STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2010M2096A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1813-2024·2024-09-25
Bliss Tree Millet Butter Recalled for Undeclared Milk Allergen
Bliss Tree Millet Butter is being recalled because it contains undeclared milk, a common allergen. The product was distributed to wholesalers and retailers in five states and to online customers nationwide.
Product
Bliss Tree Millet Butter Karasev 200g UPC:8906087451686. Packaged in a box, 13 boxes per case.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3161-2024·2024-09-25
BiomarC EX Fiducial Marker System recalled for missing MRI safety component
Carbon Medical Technologies is recalling the BiomarC EX Fiducial Marker System because patients did not receive the required MRI Insert component needed for safe use during MRI procedures.
Product
BiomarC EX Fiducial Marker System, Catalog Number 040165
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1808-2024·2024-09-25
Bliss Tree Ragi Butter Murukku recalled for undeclared milk allergen
Bliss Tree Ragi Butter Murukku 200g and 400g packages are recalled due to undeclared milk. Consumers with milk allergies should not consume these products and contact their retailer.
Product
Bliss Tree Ragi Butter Murukku 200g UPC:8906087451754. Packaged in a box, 13 boxes per case Bliss Tree Ragi Butter Murukku 400g UPC:8906087452829. Packaged in a pouch, 8 pouches per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3142-2024·2024-09-25
Alaris Pump Module 8100 Recalled for Bent Connector That May Disable Device
CareFusion is recalling approximately 192,964 Alaris Pump Module Model 8100 infusion pumps that may have bent female connectors preventing device operation and delaying patient treatment.
Product
Alaris Pump Module Model 8100, a modular infusion pump and monitoring system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3176-2024·2024-09-25
Hemodialysis bloodline connector insertion defect may cause flow restriction
B Braun Medical is recalling hemodialysis bloodline tubing because the patient connector may not fully insert into the device, potentially blocking blood flow and delaying treatment. Affected units were distributed nationwide.
Product
STREAMLINE BLOODLINE LONG VERSION, FMC-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095L
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3164-2024·2024-09-25
Endo Retrieval Pouches Recalled; Tube May Detach During Endoscopic Use
Endo retrieval pouches are recalled because the tube may detach and fall into the surgical site during use. Approximately 81,241 units distributed in Georgia, Missouri, and Pennsylvania are affected.
Product
1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2000, 5" x 7", sterile; 3. Tech Medical Services, Inc. Detachable Endo Retrieval Pouch, REF TM2002, 8" x 10", s
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1811-2024·2024-09-25
Moringa Butter Murukku Recalled for Undeclared Milk Allergen
Bliss Tree Moringa Butter Murukku 400g is recalled because it contains undeclared milk, a common food allergen. Consumers with milk allergies should not consume this product.
Product
Bliss Tree Moringa Butter Murukku 400g UPC:8906087452836. Packaged in pouches, 8 pouches per case.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1814-2024·2024-09-25
Kodiak Protein-Packed Power Waffles Recalled for Plastic Film Contamination
Kodiak Cakes LLC is recalling 7,300 boxes of Kodiak Protein-Packed Power Waffles due to soft plastic film contamination. Consumers should not consume the affected product.
Product
KODIAK PROTEIN-PACKED POWER WAFFLES BUTTERMILK & VANILLA NET WT 3.35 lb (53.6oz) 1.52kgCreated & distributed by: KODIAK CAKES PARK CITY, UT 84098 UPC 7 05599 01920 3
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-3175-2024·2024-09-25
Hemodialysis bloodline tubing recalled for improper connector insertion risk
B. Braun is recalling approximately 4.98 million STREAMLINE FRESENIUS FOR DAVITA hemodialysis bloodline tubes due to risk of improper connector insertion, which could cause blood flow occlusion during dialysis treatment.
Product
STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095DA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1812-2024·2024-09-25
Curry Leaves Snack Recalled Due to Undeclared Milk Allergen
Bliss Tree Curry Leaves Butter Murukku is recalled due to undeclared milk. The product was distributed to retailers in CA, NJ, GA, AZ, MD, and nationwide online.
Product
Bliss Tree Curry Leaves Butter Murukku 400g UPC:8906087452867. Packaged in pouches, 8 pouches per case.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3143-2024·2024-09-25
Seer Home EEG System Recalled for EMC Non-Compliance
Seer Home System ambulatory EEG devices were recalled due to electromagnetic compatibility non-compliance and manufacturing control deficiencies. The issue may affect signal recording reliability in home EEG monitoring.
Product
Seer Home System is an ambulatory electroencephalograph (EEG) system intended for at-home use for extended EEG and video EEG (vEEG) recordings and analysis. The Seer Home System includes the Sight Monitoring Hub, the Sense wearable, Monitoring Portal and associated accessory comp
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3186-2024·2024-09-25
VariSoft Infusion Sets recalled due to incorrect secondary packaging
Unomedical A/S is recalling specific VariSoft Infusion Sets packaged in boxes incorrectly branded as 'Trusteel Infusion Set' instead of 'VariSoft.' No injuries or illnesses have been reported.
Product
VariSoft Infusion Set, Single Use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3154-2024·2024-09-25
McKesson 60 mL Syringes Recalled Lacking FDA Clearance
Cypress Medical Products is recalling McKesson 60 mL syringes that lack FDA clearance. The syringes were inadvertently shipped from a distribution center due to an order processing error and were on quarantine.
Product
General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson Brand Catalog Number: 102-S60C
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3184-2024·2024-09-25
BinaxNOW Respiratory Strep A Test Kits Shipped to Unlicensed Purchasers
Cypress Medical Products is recalling BinaxNOW Respiratory Strep A Test Kits due to an inventory system error that resulted in shipment to customers without proper licensing to purchase medical devices.
Product
BinaxNOW Respiratory Strep A Test Kit, CLIA Waived, Catalog Number 730025
Category
Medical Device
Distribution
Distributed nationwide