Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

13851–13875 of 89754

HighFDA (Devices)·Z-1309-2024·2024-03-27
Nautilus ECMO Oxygenator recalled due to heat exchanger water path restriction
Mc3 Inc recalls Nautilus ECMO Oxygenator units due to heat exchanger water path restriction that degrades temperature control performance. Inadequate heat transfer may lead to hypothermia risk.
Product
NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: (1) 48145; (2) 48145E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1319-2024·2024-03-27
I.B.S. 6.5-C Compression Screw Batch Recalled for Dimensional Mix-Up
A batch of I.B.S compression screws may have incorrect dimensions compared to their labels due to a batch mix-up. The 59 affected units were distributed nationwide in Tennessee.
Product
I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 75mm,Part Number S65 ST175
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1322-2024·2024-03-27
Dental Implant Impression Coping Recalled for Manufacturing Defect
Thommen Medical AG is recalling impression coping units because the internal canal depth was not manufactured according to specifications, preventing firm connection to the dental implant. The product was distributed in Ohio and Kentucky.
Product
impression coping, repositionable, short, screw-retained, PF 4.0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2024·2024-03-27
Nasal Intubation Kit Recalled for Incompatible Tube Holder
Curaplex Nasal Intubation Kit recalled because the included endotracheal tube holder is incompatible with nasal intubation procedures, preventing practitioners from properly securing the tube.
Product
Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023060S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1340-2024·2024-03-27
Vascular Guidewire Introducer Recalled Due to Internal Hub Defect
A vascular guidewire introducer is recalled because internal voids in the hub may prevent proper guidewire passage, potentially delaying surgical procedures.
Product
MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-758
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1317-2024·2024-03-27
Medtronic Abre Venous Stent System Recalled for Sterile Package Breach
Medtronic is recalling Abre Venous Self-expanding Stent Systems due to a potential for sterile package breach. The recalled systems consist of three product numbers totaling 65 units distributed worldwide. No injuries have been reported.
Product
Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1337-2024·2024-03-27
Guidewire Introducer Recalled for Manufacturing Defect Affecting Device Function
Angiodynamics is recalling 58 units of its MINI STICK MAX guidewire introducer due to voids in the internal lumen that may prevent proper guidewire passage. Users may experience procedural delay requiring device exchange.
Product
MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-752
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1093-2024·2024-03-27
La Fiesta ground cinnamon recalled due to elevated lead levels
La Fiesta ground cinnamon (Canela Molida) is being recalled due to elevated lead levels. Affected products are 0.87oz bags with lot code 25033, distributed to retailers in California, Arizona, Washington, and Texas.
Product
La Fiesta, Canela Molida, Cinnamon Ground, 0.87oz (24.8g), UPC #032327000449, packed in cello bags
Category
Food
Distribution
4 states
SevereNHTSA·24V230000·2024-03-25
Doosan Portable Generator Trailers Recalled for Brake Wiring Defect
Doosan is recalling 2015-2023 Portable Generator Trailers because the electric brake harness was incorrectly wired, potentially disabling brakes.
Product
DOOSAN PORTABLE POWER — DOOSAN PORTABLE POWER MOBILE GENERATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V225000·2024-03-24
Mercedes-Benz Recalls 2023 Sprinter Vans for Electrical Fire Risk
Daimler Vans USA is recalling 2023 Mercedes-Benz Sprinter vans because a 12-volt ground connection may overheat, increasing the risk of fire or loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 3500, SPRINTER 2500, SPRINTER 4500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V226000·2024-03-22
Ford Recalls 2023-2024 Transit Vehicles for Tire Contact Defect
Ford is recalling 2023-2024 Transit vehicles with the Trail package because tires may contact the wheel arch liner, risking tire damage and loss of control.
Product
FORD — FORD TRANSIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V223000·2024-03-22
Ford Maverick and Bronco Sport tires may have been manufactured incorrectly
Ford is recalling certain 2023 Maverick and Bronco Sport vehicles because the tires may have been manufactured incorrectly, which may result in a loss of vehicle handling and control.
Product
FORD — FORD MAVERICK, BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V229000·2024-03-22
Audi Recalls E-Tron GT Models Due to High-Voltage Battery Fire Risk
Volkswagen Group of America is recalling 2022-2023 Audi E-Tron GT and RS E-Tron GT vehicles because a high-voltage battery short circuit could cause a fire.
Product
AUDI — AUDI E-TRON GT, RS E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V228000·2024-03-22
Audi e-tron GT high voltage battery modules may short circuit
Volkswagen is recalling certain 2022-2024 Audi RS e-tron GT and e-tron GT vehicles because the high-voltage battery may experience a short circuit within the battery modules.
Product
AUDI — AUDI E-TRON GT, RS E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V222000·2024-03-22
Reading Truck Equipment Recalls 2021-2024 Dump Trucks Due to Fire Risk
Reading Truck Equipment is recalling 2021-2024 dump body trucks because inadequate clearance may allow the hood to contact the main electrical fuse terminal, increasing the risk of a fire.
Product
READING TRUCK EQUIPMENT — READING TRUCK EQUIPMENT DUMP BODIED TRUCKS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24E028000·2024-03-22
Suburban Recalls Slide-In Ranges with Overheating LED Backlight Boards
Suburban is recalling certain Slide-In Range models because the LED backlight circuit board may overheat, increasing the risk of a fire.
Product
EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V224000·2024-03-22
Mercedes-Benz Recalls 2024 E-Class Vehicles for Wiring Harness Defect
Mercedes-Benz is recalling 2024 E350 and E450 vehicles because the transmission wiring harness may be routed too close to the driveshaft, potentially causing a loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ E 350, E 450
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V227000·2024-03-22
Subaru Outback and Legacy occupant sensors may prevent airbag deployment
Subaru is recalling certain 2020-2022 Outback and Legacy vehicles because an Occupant Detection System capacitor may crack and short circuit, preventing front passenger airbag deployment.
Product
SUBARU — SUBARU LEGACY, OUTBACK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V220000·2024-03-22
Ford Mustang low pressure fuel supply lines may be damaged or cut
Ford is recalling certain 2024 Mustang vehicles with 2.3L engines because the low-pressure fuel supply line may be damaged or cut, which can result in a fuel leak.
Product
FORD — FORD MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·24169·2024-03-21
Happiness USA Roller Ball Candy Recalled Due to Choking Hazard
Twenty Four Six Foods LLC is recalling all flavors of Happiness USA Liquid Rolling Candy because the rolling ball applicator can dislodge into a child's mouth, posing a choking hazard and risk of death.
Product
Happiness USA Liquid Rolling Candy
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24171·2024-03-21
Starbucks-branded metallic mugs recalled due to burn and laceration hazards
Nestlé USA recalls about 440,500 metallic mugs from 2023 holiday Starbucks gift sets sold at Target, Walmart, and military retailers. The mugs can overheat or break when microwaved or filled with extremely hot liquid, causing severe burns and cuts. 10 people have been injured in 12 reported incidents.
Product
Metallic Mugs included in 2023 Holiday Starbucks-branded Gift Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V221000·2024-03-21
Kawasaki Recalls 2023-2024 Ninja Motorcycles Due to Spark Plug Defect
Kawasaki is recalling 1,579 motorcycles because damaged spark plugs can cause engine stalling, increasing crash risk.
Product
KAWASAKI — KAWASAKI ZX400P, ZX400S, NINJA ZX-4RR
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-03212024-01·2024-03-21
USDA Issues Public Health Alert for Ineligible Frozen Pangasius Maws
USDA FSIS issued a public health alert for frozen striped pangasius maws illegally imported from China. The products are ineligible for entry and unfit for human consumption.
Product
FSIS Issues Public Health Alert for Ineligible Frozen Siluriformes Products Imported from the People’s Republic of China
Category
Food
Distribution
Distributed nationwide
HighNHTSA·24V219000·2024-03-21
Lamborghini Recalls 2024 Huracan Vehicles Due to High Beam Headlight Defect
Lamborghini is recalling 2024 Huracan vehicles because the high beam headlights may not activate, which can reduce visibility and increase crash risk.
Product
LAMBORGHINI — LAMBORGHINI HURACAN
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24166·2024-03-21
Culture Kings Sneaker Basel Magnetic Levitation Displays Recalled for Laceration and Ingestion Hazards
Culture Kings is recalling approximately 4,300 Sneaker Basel Magnetic Levitation Displays sold online from July 2020 through January 2023. The high-powered magnets can break and cause lacerations, or be swallowed and lodge in the digestive system, risking serious injury and death.
Product
Sneaker Basel Double Magnetic Levitation Displays
Category
Consumer Product
Distribution
Distributed nationwide

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