Recalls in Nebraska (page 28)
3895 recalls.
- Discount Drug Mart Food Market recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - caring mill recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - exchange select recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - exchange select recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - SLMD Benzoyl Peroxide Acne Lotion recall (Owen Biosciences Inc.)
DrugClass IIReported April 22, 2026 · Chemical contamination: Presence of benzene - SLMD BP Acne Spot Treatment recall (Owen Biosciences Inc.)
DrugClass IIReported April 22, 2026 · Chemical contamination: Presence of benzene - HydroPeptide CLEAR ALLIANCE SERUM recall (Owen Biosciences Inc.)
DrugClass IIReported April 22, 2026 · Chemical contamination: Presence of benzene - FHF Farmhouse Fresh recall (Owen Biosciences Inc.)
DrugClass IIReported April 22, 2026 · Chemical contamination: Presence of benzene - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported April 22, 2026 · CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported April 22, 2026 · CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported April 22, 2026 · CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit - Philips Spectral CT on Rails. Model Number: 728334. recall (PHILIPS MEDICAL SYSTEMS)
Medical deviceClass IIReported April 22, 2026 · Philips has identified three software issues: 1. During a continuous CT (CCT) scan, there is the potential that the Gantry could remain at the current scan... - CENTURION Circumcision Kit recall (Medline Industries, LP)
Medical deviceClass IIReported April 22, 2026 · On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile. - Gentuity HF-OCT Imaging System Model G10-01 recall (Gentuity, LLC)
Medical deviceClass IIReported April 22, 2026 · The potential for repeated frames during HF-OCT pullback when using the Gentuity HF-OCT Console (software version 21.11 to 23.3.13) with the Vis-Rx and Vis-Rx... - Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL... recall (Clariance-SAS)
Medical deviceClass IIReported April 22, 2026 · Due to a quality issue regarding the presence of burr on the finished cervical plate product. - React Health PHOENIX 5L Oxygen Concentrator recall (3B Medical, Inc.)
Medical deviceClass IIReported April 22, 2026 · Devices which did not meet internal quality specifications were inadvertently distributed. - Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only recall (Wilson-Cook Medical Inc.)
Medical deviceClass IIReported April 22, 2026 · Due to increased in complaints their is the potential for endoscopic clipping device to malfunction. - Arjo Tenor mobile passive patient lift recall (ARJOHUNTLEIGH POLSKA Sp. z.o.o.)
Medical deviceClass IIReported April 22, 2026 · An internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case... - LinkBio CORE Workstation recall (Linkbio Corp.)
Medical deviceClass IIReported April 22, 2026 · The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen. - Yeastone Broth recall (Remel, Inc)
Medical deviceClass IIReported April 22, 2026 · Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal... - Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 22, 2026 · Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool). Philips has determined that the MAFA... - B Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Barun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7 recall (Insulet Corporation)
Medical deviceClass IReported April 22, 2026 · Due to a manufacturing defect, certain Omnipod 5 Pods from 49 lots have an internal soft cannula tear that results in insulin leaking into the Pod instead of... - JC Sales Recalls Lil' Buddies Pet Laser Toys Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported April 17, 2026 · The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate... - Montessori Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Mandatory Standard for Teething Toys; Sold on Amazon by SpringFlower
Consumer productReported April 17, 2026 · The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate... - Apex Gaming PCs Recalls Manik and Apex-branded ATX Computer Power Supplies Due to Risk of Serious Injury or Death from Electrical Shock and Electrocution Hazards
Consumer productReported April 17, 2026 · The units lack a permanent, on-product warning label identifying potential electrical shock and electrocution hazards, posing a risk of serious injury or death... - Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by ZOLIQUEX
Consumer productReported April 17, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - ZMC Group Recalls LED Finger Beam Lights Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
Consumer productReported April 17, 2026 · The recalled toys violate the mandatory safety standard for children's toys because the toy contains button cell batteries that can be easily accessed by... - Sweetcrispy Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Consumer productReported April 17, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution... - Le Hao Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Consumer productReported April 17, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution... - Fengrong Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Consumer productReported April 17, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution... - Agiiman Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Consumer productReported April 17, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution. - Free-Standing Professional Gas Ranges Recalled Due to Risk of Burn Hazard; Manufactured by Fisher & Paykel
Consumer productReported April 17, 2026 · The ovens in the ranges can experience a delayed ignition, causing gas to accumulate and the oven door to open from combustion, posing a burn hazard to users. - Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by Patoolio Direct
Consumer productReported April 17, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution... - Mini Round Toddler Trampolines Recalled Due to Strangulation Hazard; Risk of Serious Injury or Death; Manufactured by SEGMART
Consumer productReported April 17, 2026 · Young children can become entangled in the straps of the hammock, punching bag and hand ring accessories, posing a strangulation hazard, which can result in... - Fun and Function Recalls Children's Metal Multi-Point Swing Frames Due to Risk of Injury from Fall Hazard
Consumer productReported April 17, 2026 · The swing frames can crack or break during use, posing a fall hazard, which can result in injury. - Macy's Recalls Arch Studio Tea Kettles Due to Risk of Serious Injury from Burn Hazard
Consumer productReported April 17, 2026 · The tea kettles' handle can detach during use when heated, posing a risk of serious injury from burn hazard. - ATOYUS Children's Activity Cubes Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban and Mandatory Standard for Toys; Sold on Amazon by Melofaver US
Consumer productReported April 17, 2026 · The recalled toys violate the small parts ban because the toys are intended for children under three and the toys' xylophone screws and clock hands can detach.... - nvyue Magic Pocket Staffs Recalled Due to Projectile and Laceration Hazards; Imported by Xingwenfeng
Consumer productReported April 17, 2026 · The protective pin mechanism on the Magic Pocket Staffs can fail to prevent unintentional expansion, posing serious projectile and laceration hazards. Even... - Sanlebi Pet Vet Playsets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Letokids
Consumer productReported April 17, 2026 · The Pet Vet Playset violates the mandatory standard for toys because the button cell batteries in the nail grinder and otoscope can be easily accessed by... - Generac Power Systems Recalls Portable Generators Due to Risk of Serious Injury or Death from Burn and Fire Hazards
Consumer productReported April 17, 2026 · When first filling the recalled generator with gasoline, fuel can leak from the carburetor, posing a risk of serious injury or death from fire or burn hazard.... - Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by BAYOTAK USA
Consumer productReported April 17, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution... - Stryker Sustainability Solution Color Cuff 24" recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported April 15, 2026 · Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure. - Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat recall (Tornier, Inc)
Medical deviceClass IIReported April 15, 2026 · Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with... - GE Healthcare Omnipaque recall (GE Healthcare Ireland Limited)
DrugClass IIReported April 15, 2026 · Presence of particulate matter - GE Healthcare Omnipaque recall (GE Healthcare Ireland Limited)
DrugClass IIReported April 15, 2026 · Presence of particulate matter - Xanax XR recall (Viatris, Inc.)
DrugClass IIReported April 15, 2026 · Failed Dissolution Specifications - Artificial Tears Lubricant Eye Drops recall (Preferred Pharmaceuticals, Inc.)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - Vancomycin HCL recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port - Vancomycin HCI recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port - Vancomycin HCI recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port - norepinephrine Bitartrate recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port - norepinephrine Bitartrate recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port - 5% Dextrose Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 5% Dextrose Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 5% Dextrose Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - 0.45% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - Lanreotide Injection recall (Cipla USA, Inc.)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure. - Lanreotide Injection recall (Cipla USA, Inc.)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure. - Multi-parameter Command Module recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported April 15, 2026 · Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve... - See Luer Cap Set recall (Molded Products Inc)
Medical deviceClass IIReported April 15, 2026 · Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Control Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - ARTIS pheno and ARTIS Icono biplane recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported April 15, 2026 · During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing... - Muscccm Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by SZ Hengxun
Consumer productReported April 10, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - Prestige Import Group Recalls Supernova and Typhoon Lighters Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Cigarette Lighters
Consumer productReported April 10, 2026 · The recalled lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanism, posing a risk of... - LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries; Sold on Amazon by Happiness Light
Consumer productReported April 10, 2026 · The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin... - Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords Recalled Due to Risk of Serious Injury and Death from Electrocution and Carbon Monoxide Poisoning Hazards; Sold on Walmart
Consumer productReported April 10, 2026 · The recalled male-to-male extension cords violate safety requirements because their exposed prongs can become energized when one end is plugged into a...