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 deaths or serious injuries are reported, 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

10501–10525 of 27647

HighFDA (Devices)·Z-0019-2025·2024-10-09
Hemodialysis console blood leak sensor may fail to trigger alarm
A component in certain Tablo Hemodialysis consoles may fail to detect small blood leaks promptly, potentially causing symptoms like hypotension, fatigue, and dizziness if undetected blood loss occurs.
Product
Tablo Console, REF: PN-0003000, PN-0006000, part of the Tablo Hemodialysis System. The Tablo Hemodialysis System is indicated for use in patients with acute and/or chronic renal failure, with or without ultrafiltration, in an acute or chronic care facility.
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-3308-2024·2024-10-09
DVOT Rapid Antigen Test Kits Recalled for Lack of FDA Authorization
DVOT antigen test kits lack FDA authorization for US sale. Approximately 50,000 unauthorized kits were distributed. Users should discontinue use immediately due to unvalidated safety and accuracy.
Product
DVOT SARS-CoV-2 & RSV &MP &ADV & FIu A/B Antigen Combo Test Kit, Model Number ACT01
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0005-2025·2024-10-09
Sriracha Sauce Recalled for Manufacturing Without Proper Authorization
Blue Tape Sriracha sauce (136 bottles, 10.5 oz each) was manufactured without the required authorization for producing acidified foods, creating potential safety risks.
Product
Blue Tape Sriracha sauce is refrigerated condiment, packaged in a 10.5oz clear squeeze bottle, sold individually. Ingredients: Chilies, Garlic, Capsicum, Sugar, Salt, White Wine Vinegar. There is no company address on the label and no UPC code.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0020-2025·2024-10-09
Banana nut muffins recalled for undeclared milk and wheat allergens
The Posh Bakery recalls Whole Grains Bakery Banana Nut Muffins (6 oz) due to undeclared milk and wheat allergens. The muffins lack required allergen-contains statements and nutritional fact labels.
Product
Whole Grains Bakery labeled "Banana Nut Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 101 6"
Category
Food
Distribution
0 states
HighFDA (Food)·F-0017-2025·2024-10-09
Chocolate chip muffins recalled for undeclared milk and wheat
The Posh Bakery is recalling Whole Grains chocolate chip muffins due to undeclared milk and wheat allergens with missing allergen labeling. Those with milk or wheat allergies should not consume this product.
Product
Whole Grains Bakery labeled "Choclate Chip Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 105 4"
Category
Food
Distribution
0 states
HighFDA (Food)·F-1836-2024·2024-10-09
Mini Raspberry Lemon Coffee Cake Recalled for Undeclared Walnuts and Wheat
Mini Raspberry Lemon Coffee Cake products in Washington were mislabeled and contain undeclared walnuts and wheat. Consumers with allergies to these ingredients should not consume the product and should return it to the store.
Product
Mini Raspberry Lemon Coffee Cake, net wt. 13.5oz. UPC 8 57297 00745 4. Made with Gluten-Free Ingredients in a Gluten-Friendly Bakery. Macrina Bakery - Kent, WA. Ingredients: CANE SUGAR, GREEK YOGURT (GRADE A PASTEURIZED CULTURED MILK, CREAM, NONFAT MILK), EGGS, RASPBERRIES, B
Category
Food
Distribution
1 state
HighFDA (Food)·F-0022-2025·2024-10-09
Cranberry Muffins Recalled for Undeclared Milk and Wheat Allergens
The Posh Bakery is recalling Cranberry Muffins due to undeclared whey (milk) and wheat flour, as well as missing nutrition facts panel and allergen statement. Consumers with milk or wheat allergies should not consume these products.
Product
Whole Grains Bakery labeled "Cranberry Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090
Category
Food
Distribution
0 states
HighNHTSA·23V648000·2024-10-09
2024 East to West RV Recall: Detachable Rear Ladder Poses Injury Risk
Forest River is recalling certain 2024 East to West Blackthorn and Tandara fifth wheels. The rear ladder may detach due to improper anchoring, creating a potential injury risk.
Product
EAST TO WEST — 2024 EAST TO WEST BLACKTHORN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0001-2025·2024-10-09
Prescription atorvastatin bottles recalled for containing wrong medication
A carbamazepine (anticonvulsant) tablet was found in bottles of atorvastatin (cholesterol medication). The affected lot includes 2,328 bottles distributed nationwide.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3313-2024·2024-10-09
Alcon contact lenses recalled for manufacturing quality defect
Alcon is recalling approximately 92,835 packs of contact lenses because a material quality issue may affect lens performance standards. Wearers may experience temporary eye irritation, redness, or blurred vision.
Product
DAILIES TOTAL1, DAILIES TOTAL1 for Astigmatism, DAILIES TOTAL1 Multifocal, TOTAL30 Sphere,
Category
Medical Device
Distribution
51 states
HighFDA (Drugs)·D-0007-2025·2024-10-09
Pluvicto Radiopharmaceutical Drug Recalled Due to Manufacturing Quality Deviations
Advanced Accelerator Applications is recalling 99 doses of Pluvicto (lutetium LU-177 injection) due to manufacturing quality deviations. The affected lots were distributed to six states.
Product
Pluvicto, 1000 MBq/mL (27 mCi/mL), lutetium, LU 177, vipivotide tetraxetan injection, Single-dose vial, Sterile, Manufacturer Advanced Accelerator Applications, 57 E. Willow Street, NJ 07041, Millburn USA. NDC 69488-0010-61
Category
Drug
Distribution
6 states
SevereNHTSA·24V598000·2024-10-08
2020-2022 Ford Explorer Engine Compartment Fire Risk Recall
Certain 2020-2022 Ford Explorers may experience engine failures that release oil and fuel vapors, risking engine compartment fires. Ford will update the engine control software and inspect for bearing damage.
Product
FORD — 2020 FORD EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V591000·2024-10-08
Harley-Davidson Softail Motorcycles Recalled for Faulty Shock Absorber Fastener
Harley-Davidson is recalling certain 2018–2023 Softail motorcycles where a fastener securing the rear shock absorber may break, causing tire damage and loss of tire pressure. This can lead to loss of vehicle control and increased crash risk.
Product
HARLEY-DAVIDSON — 2021 HARLEY-DAVIDSON FXLRS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V330000·2024-10-05
Lincoln Corsair transmission control software defect causes unexpected neutral shift
Ford is recalling 2021-2022 Lincoln Corsair vehicles due to a hybrid powertrain control module software defect that may cause the transmission to shift into neutral unexpectedly, resulting in loss of drive power and increased crash risk.
Product
LINCOLN — 2021 LINCOLN CORSAIR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V326000·2024-10-05
2024-2025 Coachmen Nova Motorhomes: Solar Panel Detachment Risk
Forest River is recalling certain 2024-2025 Coachmen Nova Class B motorhomes because the solar panel may detach from the pop-up roof, potentially becoming a road hazard.
Product
COACHMEN — 2024 COACHMEN NOVA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V331000·2024-10-05
2022 Mercedes-Benz EQB Front Axle Drivetrain Rollaway Risk Recall
Mercedes-Benz recalls 2022 EQB 300 and 350 vehicles due to improperly welded front axle gears that may fail, causing vehicle rollaway and crash risk. Dealers will replace the front axle drivetrain free of charge.
Product
MERCEDES-BENZ — 2022 MERCEDES-BENZ EQB 300 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V328000·2024-10-05
Bus Fuel Filter Hoses May Disconnect; Fire and Stall Risk
Nova Bus is recalling certain 2022-2023 LFS buses due to secondary fuel filter hoses with insufficient crimping that may disconnect and leak. A fuel leak could cause a fire or engine stall.
Product
NOVA BUS — 2022 NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V327000·2024-10-05
2024-2025 BMW X5 Tire Placard May Display Incorrect Size and Pressure
BMW is recalling certain 2024-2025 X5 xDrive40i models because the tire information placard may display incorrect tire size and pressure, potentially leading to improper tire installation or inflation and increased crash risk.
Product
BMW — 2024 BMW X5
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3137-2024·2024-10-02
CARDIOSAVE RESCUE intra-aortic balloon pump software correction for hemodynamic instability
Datascope Corp. is issuing a software correction for CARDIOSAVE RESCUE intra-aortic balloon pump devices to address risks of hemodynamic instability and failure to properly transmit clinical data worldwide.
Product
CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic balloons.
Category
Medical Device
Distribution
0 states
SevereNHTSA·23V110000·2024-10-02
2023 Lucid Air propulsion system electrical switches may fail unexpectedly
Lucid is recalling certain 2022-2023 Air vehicles because electrically activated contactor switches in the propulsion system may unexpectedly open, cutting power to the electric motors and increasing the risk of a crash.
Product
LUCID — 2023 LUCID AIR
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3134-2024·2024-10-02
Cardiosave hybrid IABP software defect poses hemodynamic instability and data loss risk
Datascope's Cardiosave Hybrid IABP devices carry a risk of hemodynamic instability and clinical data transmission failure due to a software defect. Datascope has developed a software correction (Revision D.00) to mitigate this risk.
Product
CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic balloons.
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-3090-2024·2024-10-02
ParaPAC Plus 310 ventilator connector may detach and stop ventilation
Smiths Medical is recalling paraPAC Plus 310 ventilators because the patient outlet connector may loosen or detach, potentially interrupting ventilation. Approximately 11,244 units worldwide are affected.
Product
paraPAC plus 310 ventilator kit with internal PEEP and CPAP, Item Number P310N
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-3135-2024·2024-10-02
CARDIOSAVE Rescue IABP software defect poses hemodynamic instability risk
Datascope CARDIOSAVE Rescue IABP devices have a software defect that risks hemodynamic instability and clinical data transmission failure. A software correction is available.
Product
CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic balloons.
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-3153-2024·2024-10-02
Ivenix Infusion Pump Software Recalled for Potential Malfunctions
Fresenius Kabi is recalling Ivenix Infusion System software (Version 5.9.1 and prior) due to anomalies that can cause pump malfunctions, alarms, or unresponsive screens while delivering medication, risking serious patient harm.
Product
Ivenix Infusion System (IIS), LVP Software; LVP-SW-0004, Software Version 5.9.1 and prior. Infusion pump software for infusion management system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3201-2024·2024-10-02
Philips MR 5300 MRI System Recalled for Loose Assembly Screws
Philips is recalling 68 MR 5300 MRI diagnostic systems worldwide because loose screws in the RF carrier assembly could block equipment movement and delay patient diagnosis.
Product
MR 5300 - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782110
Category
Medical Device
Distribution
Distributed nationwide

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10501–10525 of 27647