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.
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.
Minimum severity
Ford is recalling 2021-2022 Transit and 2021 Transit Connect vehicles because the front passenger seat belt locking retractor may deactivate, preventing child restraint securement. Unsecured child restraints increase crash injury risk.
Entegra Coach is recalling certain 2018-2022 Anthem, Aspire, Insignia, and Reatta XL motorhomes. A faulty sealing washer in the fuel rail assembly may leak, creating a fire risk. Contact Entegra Coach at 1-800-517-9137 for repairs.
General Motors is recalling certain 2021 Chevrolet Tahoe and GMC Yukon vehicles because dealer technicians may have incorrectly calibrated the brake system control module, potentially compromising braking performance and stability control.
Generac is recalling about 321,160 portable generators (6500 and 8000 watt models) because an unlocked handle can pinch and amputate consumers' fingers when the generator is moved. Eight injuries have been reported, including seven finger amputations.
General Motors is recalling 2020-2021 Silverado 2500 and Sierra 2500 trucks where a 17-inch spare tire paired with larger road tires prevents ABS from engaging, raising crash risk. Dealers will replace the spare tire and label at no cost.
Shyft Group is recalling certain 2018-2022 Spartan RV Chassis models (K1, K2, K3, K4) because the instrument cluster may intermittently go blank while the vehicle is in motion, potentially obscuring critical speed and warning information.
SHEIN children's sleepwear sets fail to meet federal flammability standards and pose a burn injury risk. About 2,320 units sold online from August 2019 through January 2021 are affected.
Specialized is recalling about 2,500 first-generation Turbo Levo and Kenevo electric mountain bike battery packs because water can penetrate the seal around the LED control pad and cause the battery to short circuit, creating fire and burn hazards.
Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer Aloe Watermelon Lemonade due to contamination with methanol, benzene, and acetaldehyde. The 3.38 FL. OZ. bottles were distributed nationwide.
Nuri Trading LLC is recalling Shogun-X 7000 capsules nationwide because they contain undeclared tadalafil and sildenafil, FDA-approved prescription drugs not listed on the label, making the product an unapproved drug.
Nuri Trading LLC is recalling Thumbs Up 7 Black 25K capsules nationwide because they contain undeclared tadalafil, an FDA-approved drug. The product was marketed without required approval, making it an unapproved drug with unestablished safety and efficacy.
Shogun-X capsules have been recalled because they contain undeclared tadalafil, sildenafil, and/or vardenafil—prescription drugs not listed on the label. These are unapproved drugs whose safety and efficacy have not been established.
Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer aloe Melon Picnic spray (3.38 FL. OZ., Lot #20259) due to contamination with methanol, benzene, and acetaldehyde.
Krazy Night capsules (1-count blister cards and 10-count boxes) are being recalled nationwide because they contain undeclared tadalafil, sildenafil, and/or vardenafil without FDA approval. These unapproved drugs have not undergone safety and efficacy review.
Scentsational Soaps & Candles Inc is recalling SS Tangerine & Guava Scented Sanitizer (3.38 FL. OZ.) due to contamination with methanol, benzene, and acetaldehyde. The product was distributed nationwide.
Goose Creek Hand Sanitizer aloe Dragonfruit Splash (3.38 FL. OZ.) is being recalled because the product is contaminated with methanol, benzene, and acetaldehyde. Consumers should stop using the product immediately.
Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer aloe Grape Soda spray because it contains methanol, benzene, and acetaldehyde. The contaminated product was distributed nationwide.
Scentsational Soaps & Candles Inc is recalling SS Lavender & Herbs Scented Sanitizer due to contamination with methanol, benzene, and acetaldehyde. The affected product was distributed nationwide.
Goose Creek Hand Sanitizer aloe Red, White & Blue Anti-Bacterial Spray (3.38 FL. OZ.) is being recalled nationwide because it is contaminated with methanol, benzene, and acetaldehyde.
Nuri Trading LLC is recalling 69MODE Blue 69 capsules nationwide because they contain undeclared tadalafil and sildenafil, two FDA-approved drugs, making the product an unapproved drug without established safety or efficacy.
Ummzy LLC is recalling Thumbs Up 7 Red 70K capsules because they contain undeclared tadalafil and/or sildenafil and vardenafil, making them unapproved drugs with unestablished safety and efficacy.
Philips Respironics V60 ventilators with High Flow Therapy software versions 3.00 and 3.10 may reduce oxygen delivery below prescribed levels when pressure limits are reached, risking oxygen desaturation.
Goose Creek Hand Sanitizer aloe Marshmallows (3.38 FL. OZ.) is recalled nationwide due to contamination with methanol, benzene, and acetaldehyde. Consumers should stop using the product immediately.
Goose Creek Hand Sanitizer aloe Limoncello (100 mL) is being recalled because the product contains methanol, benzene, and acetaldehyde. Consumers should stop using the product immediately.
Respironics V60 Plus Ventilators (software versions 3.00 and 3.10) may reduce oxygen flow below clinical settings, risking oxygen desaturation and hypoxemia in mechanically ventilated patients.