Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,851 recalls, newest first · Checked 17 minutes ago
United States
Goody King Magnetic Building Cubes and Blocks Recalled Due to Risk of Serious Injury or Death from Magnetic Ingestion Hazard; Imported by Yi Suen Commerce
The recalled magnetic building cubes contain magnets that can become loose if the cubes break or open, posing a magnet ingestion hazard to children.
GigaCloud Technology USA Recalls Merax Murphy Beds Due to Risk of Serious Injury or Death from Impact and Crush Hazards
During assembly or disassembly, the frame of the wall bed can fall onto consumers, posing deadly impact, crush and laceration hazards.
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
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 risk of…
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
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 death to…
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
The recalled fuel containers violate the requirement for closures under the Children's Gasoline Burn Prevention Act.
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
The recalled magnetic cubes violate the mandatory standard for toys because the cubes were packaged with loose high-powered magnets, posing an ingestion hazard to…
Cooluli Recalls 10-Liter and 15-Liter Minifridges Due to Fire and Burn Hazards
The recalled minifridges' electrical switch can short circuit, posing fire and burn hazards.
COMMOWNER Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by AZ Home Concept
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 extension cord…2024-2026 X3 sDrive30i and other models recall: Incorrectly attached steering spindle
An incorrectly attached steering spindle can lead to a loss of steering control, increasing the risk of a crash.2022-2026 840i and other models recall: Loss of rear wheel power from driveshaft damage
An unexpected loss of drive power can increase the risk of a crash.Grote replacement marker lights with part number 78513681 recall: Marker lights may fail to Illuminate/FMVSS 108
Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.hybrid systems with part numbers evAPU and other models recall: High voltage battery may fail and cause fire
Battery failure can also increase the risk of a fire.Grote replacement marker lights with part number 78513681 recall: Marker lights may fail to Illuminate/FMVSS 108
Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.Maquet Critical Care AB recalls Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i…
Events observed where anesthetic agent was not delivered when the vaporizer was activated.Siemens Healthcare Diagnostics, Inc. recalls Syva Emit Disopyramide Assay Enzyme Immunoassay
Out-of-specification sodium azide concentration in Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1.Contego Medical, Inc recalls Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated…
Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter, that due to a wire-to-filter-bond issue, may fail to…Philips Medical Systems Nederland B.V. recalls Philips Allura under the following System Descriptions and corresponding model numbers… and 2 more products
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.Nuclein LLC recalls Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument…
Due to a software issue which may result in false co-infection (e.g., Positive for Flu A, when SARS-CoV-2 is present).Therabody, Inc recalls Charger for the Therabody Theragun
Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire).Beckman Coulter Biomedical GmbH recalls REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info…
Due to software issues where does not handle combo assay results.Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence…
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.Hardy Diagnostics recalls HardyDisk AST Cefiderocol 30¿g
Due to incorrect cartridges include in affected products that there is the potential for false-susceptible or false-resistant susceptibility results and may lead to…Biofire Defense recalls FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code:
Firm has identified mismatches between the outbreak strain and the reference strain used in the development of its qualitative, multiplexed, nucleic acid-based in vitro…A little guidance
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Recall classes explained: Class I, II and III
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What to do if something you own is recalled
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