Recalls in Nebraska (page 11)
3895 recalls.
- Boston Scientific ENROUTE Transcarotid Neuroprotection System recall (Boston Scientific Corporation)
Medical deviceClass IReported August 26, 2026 · Potential for arterial sheath tip separation or partial tip separation during use. - Beckman Coulter recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported August 26, 2026 · Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine... - Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported August 26, 2026 · Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine... - Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software version 1.5 or... recall (Beckman Coulter Inc.)
Medical deviceClass IIReported August 26, 2026 · a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by... - Beckman Coulter DxC 500i Clinical Analyzer Modules using software version 1.5 or... recall (Beckman Coulter Inc.)
Medical deviceClass IIReported August 26, 2026 · a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by... - Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A recall (Paragon 28, Inc.)
Medical deviceClass IIIReported August 26, 2026 · Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility. - Custom Made Device Implant 6123 Navicular Cage Small Right Rev A recall (Paragon 28, Inc.)
Medical deviceClass IIIReported August 26, 2026 · Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility. - Blanketrol III recall (Gentherm Medical, LLC)
Medical deviceClass IIReported August 26, 2026 · Overheating of the 115V CPU board may cause the device to shut down. - Innercool Coolblue Console recall (Gentherm Medical, LLC)
Medical deviceClass IIReported August 26, 2026 · Overheating of the 115V CPU board may cause the device to shut down. - Blanketrol II Model 222S recall (Gentherm Medical, LLC)
Medical deviceClass IIReported August 26, 2026 · Overheating of the 115V CPU board may cause the device to shut down. - Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF recall (Siemens Healthcare Diagnostics Products Ltd.)
Medical deviceClass IIReported August 26, 2026 · Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive. - Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF:L2KSY2 recall (Siemens Healthcare Diagnostics Products Ltd.)
Medical deviceClass IIReported August 26, 2026 · Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive. - Halyard LAVH PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported August 26, 2026 · The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit. - GETINGE Y SENSOR Module recall (Maquet Critical Care AB)
Medical deviceClass IIReported August 26, 2026 · The module did not undergo electrical safety tests and functional tests during production. - Suture Cinch Long 1pk. Endoscopic tissue approximation device. recall (Boston Scientific Corporation)
Medical deviceClass IIReported August 26, 2026 · Device may fail to deploy the cinch implant and/or fail to cut the suture as intended. - OverStitch Suture Cinch recall (Boston Scientific Corporation)
Medical deviceClass IIReported August 26, 2026 · Device may fail to deploy the cinch implant and/or fail to cut the suture as intended. - TD Navio Maxi Speech Generating Device Model/Catalog Number: 1000799 recall (Tobii Dynavox Llc)
Medical deviceClass IIReported August 26, 2026 · Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an... - TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798 recall (Tobii Dynavox Llc)
Medical deviceClass IIReported August 26, 2026 · Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an... - Arrow-LOK Implant recall (Arrowhead DE LLC)
Medical deviceClass IIReported August 26, 2026 · Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection. - Cardiac Workstation 7000. Product Number: 860441. recall (Philips North America Llc)
Medical deviceClass IIReported August 26, 2026 · Device will intermittently provide inaccurate data related to native heart rate. - Cardiac Workstation 5000. Product Number: 860439. recall (Philips North America Llc)
Medical deviceClass IIReported August 26, 2026 · Device will intermittently provide inaccurate data related to native heart rate. - One-Piece Guedel Airway recall (Intersurgical Inc)
Medical deviceClass IIReported August 26, 2026 · Devices could potentially be occluded or partially occluded. - One-Piece Guedel Airway recall (Intersurgical Inc)
Medical deviceClass IIReported August 26, 2026 · Devices could potentially be occluded or partially occluded. - Hamilton Microlab STAR Liquid Handler recall (Foundation Medicine, Inc.)
Medical deviceClass IIReported August 26, 2026 · Software issue that can cause an increase in spontaneous software closures. - CCM Hockey U.S. Recalls FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories Due to Risk of Injury from Laceration or Impact Hazards
Consumer productReported August 20, 2026 · The recalled hockey visors and replacement visor accessories can crack upon impact, posing a risk of injury due to laceration or impact hazards. - Workbless Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards
Consumer productReported August 20, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or... - Koorlian Mattresses Recalled Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability; Sold on Amazon by Dream Bedding Technology
Consumer productReported August 20, 2026 · The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire. - JINHEZO Mini Waterproof LED Tea Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Imported by Mystic ZO
Consumer productReported August 20, 2026 · The LED Tea Lights violate the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed... - Goal Zero Recalls YETI 3000X Power Stations Due to Serious Risk of Injury from Fire and Burn Hazards
Consumer productReported August 20, 2026 · The recalled power station's circuit board can overheat, posing a risk of serious injury from fire and burn hazards. - Modine Manufacturing Company Recalls Airedale Heating and Cooling Ventilation Fans Due to Fire Hazard
Consumer productReported August 20, 2026 · The ventilation fan motor in the heat pumps can short circuit if water gets on the circuit board, causing the units to overheat and posing a fire hazard. - KTM North America Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death from Crash Hazard
Consumer productReported August 20, 2026 · The rear brake caliper can crack or break, reducing the brake system's effectiveness, posing a risk of serious injury or death due to crash hazard. - Aquafaba Powder recall (529 COMMERCE, LLC)
FoodClass IReported August 19, 2026 · Undeclared Egg - ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000 recall (Erbe USA Inc)
Medical deviceClass IIReported August 19, 2026 · A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in... - Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 ... recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported August 19, 2026 · Due to off-the-shelf display port component that has audio/video failures - Cefazolin in Dextrose recall (Baxter Healthcare Corporation)
DrugClass IReported August 19, 2026 · Presence of Particulate Matter - Optiray Imaging Bulk Package-350 recall (Liebel-Flarsheim Company LLC)
DrugClass IReported August 19, 2026 · Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass. - Glutathione recall (Victory Medical Center Pharmacy)
DrugClass IReported August 19, 2026 · Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. - CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION recall (Heritage Pharmaceuticals Inc)
DrugClass IIReported August 19, 2026 · Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles. - CLEAR EYES Maximum Itchy Eye Relief recall (Prestige Brands Holdings)
DrugClass IIReported August 19, 2026 · Lack of assurance of sterility. The recall is due to potential contamination - SILDENAFIL CITRATE USP recall (Shoolin Pharma Chem LLP)
DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection - TADALAFIL USP recall (Shoolin Pharma Chem LLP)
DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection - TADALAFIL USP recall (Shoolin Pharma Chem LLP)
DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection - TADALAFIL USP recall (Shoolin Pharma Chem LLP)
DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection - SILDENAFIL CITRATE USP recall (Shoolin Pharma Chem LLP)
DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection - SEMAGLUTIDE 20mg recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 10mg recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 7.5mg recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 5mg recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 2.5mg recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 0.9mg recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 9mg recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 4.5mg recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 6.75mg recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 2.25MG recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - SEMAGLUTIDE 12.5MG recall (Apollo Care, LLC)
DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material - Diovan recall (Novartis Pharmaceuticals Corporation)
DrugClass IIReported August 19, 2026 · Failed Dissolution Specifications - Cardinal Health Presource Kits: 1) BASIC PACK recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. - Cardinal Health Presource Kits: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. - Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. - Cardinal Health Presource Kits: 1) SEPTO RHINO PACK recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. - Cardinal Health Presource Kits: 1) ENT TRAY recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. - Cardinal Health Presource Kits: 1) NEWNAN SMR PACK recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. - Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. - Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. - BIOFIRE Respiratory Panel 2.1 recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported August 19, 2026 · Due to increase in false negative results - Straumann Bone Level Tapered recall (Straumann USA LLC)
Medical deviceClass IIReported August 19, 2026 · Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the... - OBP Medical recall (OBP Medical Corporation)
Medical deviceClass IIReported August 19, 2026 · There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both... - GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. ... recall (Terumo Medical Corporation)
Medical deviceClass IIReported August 19, 2026 · Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire. - GM Helix Implant recall (Straumann USA LLC)
Medical deviceClass IIReported August 19, 2026 · There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect... - Allura Xper FD. Model Numbers: 722026 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 19, 2026 · Firmware issue potentially leading to loss of geometry movements. - Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL recall (Remel Europe Ltd.)
Medical deviceClass IIReported August 19, 2026 · Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds. - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623 recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING ... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 ... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP recall (Galt Medical Corporation)
Medical deviceClass IIReported August 19, 2026 · Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits. - GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported August 19, 2026 · 10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes... - GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported August 19, 2026 · 10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes... - navify Digital Pathology recall (Ventana Medical Systems, Inc.)
Medical deviceClass IIReported August 19, 2026 · Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window - BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL ... recall (MICROVENTION INC.)
Medical deviceClass IIReported August 19, 2026 · Due to an increase rate of balloon pinhole defects. - Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall (Baxter Healthcare Corporation)
Medical deviceClass IReported August 19, 2026 · Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open... - Hampton Bay Halwin 52-Inch Ceiling Fans Recalled Due to Impact and Injury Hazards; Manufactured by Youngo Limited
Consumer productReported August 14, 2026 · The fan blades can separate from the fan motor flywheel, posing impact and injury hazards to consumers. - Sunnyside Corporation Recalls 1-K Kerosene Heater and Appliance Fuel Containers Due to Risk of Serious Injury or Death from Flash Fire and Burn Hazard; Violates Mandatory Standards for Portable Fuel Containers
Consumer productReported August 14, 2026 · The pre-filled fuel containers violate the mandatory safety standards of the Portable Fuel Container Safety Act because they lack flame mitigation devices... - Fastbuy Recalls Zimtown Portable Gas and Fuel Cans Due to Risk of Serious Injury or Death from Burn Hazard and Child Poisoning; Violate Mandatory Standard for Portable Fuel Containers
Consumer productReported August 14, 2026 · The fuel containers violate the requirement for closures under the Children's Gasoline Burn Prevention Act because the closure is not child-resistant, posing a... - SUGIFT Recalls SUGIFT Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Consumer productReported August 14, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and, because the power cord is short, it may encourage use of an... - CuberShop Magnetic Speed Cubes Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Imported by SKY CUBE HK
Consumer productReported August 14, 2026 · The recalled magnetic cubes violate the mandatory standard for toys because the cubes were packaged with loose high-powered magnets, posing an ingestion hazard... - Shengsen Prank Sound Makers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries; Imported by Shengsen Toys
Consumer productReported August 14, 2026 · The recalled sound maker violates the mandatory safety standard for consumer products with button cell and coin batteries because the lithium coin batteries... - Ritchey Design Recalls Carbon Bicycle Forks Due to Risk of Serious Injury or Death from Fall and Crash Hazards
Consumer productReported August 14, 2026 · The alloy insert located in the front crown hole of the carbon fork can come loose, causing an accessory to fall off and land on the bike's front wheel, posing... - Mattresses Recalled Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability; Sold on Amazon by Qabefy
Consumer productReported August 14, 2026 · The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire. - GigaCloud Technology USA Recalls Merax Murphy Beds Due to Risk of Serious Injury or Death from Impact and Crush Hazards
Consumer productReported August 14, 2026 · During assembly or disassembly, the frame of the wall bed can fall onto consumers, posing deadly impact, crush and laceration hazards. - Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash Hazard; Violates Mandatory Standard for ATVs
Consumer productReported August 14, 2026 · The recalled youth ATVs violate the mandatory safety standard for ATVs because the parking brakes fail to hold and the ATV's speed limiting device is not set... - COMMOWNER Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by AZ Home Concept
Consumer productReported August 14, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and, because the power cord is short, it may encourage use of an... - Deli Jerry Fuel Containers Recalled Due to Risk of Serious Injury or Death from Burn Hazard and Child Poisoning; Violate Mandatory Standard for Portable Fuel Containers; Sold on Walmart.com by Deli OfficeSupplies
Consumer productReported August 14, 2026 · The recalled fuel containers violate the requirement for closures under the Children's Gasoline Burn Prevention Act. The closure is not child-resistant, posing... - DUMOS Nine-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported August 14, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - TooyBing Wooden Bead Stacking Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Small Parts Ban
Consumer productReported August 14, 2026 · The recalled toys violate the small parts ban because they are intended for children under three years old and the wooden beads pose a deadly choking hazard to...