305 recalls tagged with “federal law violation”.
Samson International is recalling Bellevue and Oaklynn canopy bed frames sold under the Universal Broadmoor brand. The canopy beams can collapse when the bed is moved, posing an impact and injury risk. Stop using the bed immediately and contact Samson for a free repair kit that includes four mounting brackets and hardware.
F&S Fresh Foods recalled 325 ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwiches distributed in Oregon after sesame was not declared on the label. The issue involves sesame as an undeclared allergen in a product labeled to contain egg, milk, soy, and wheat. Consumers should not eat the sandwich and should contact F&S Fresh Foods for refunds or replacements.
House of Flavors recalled 4,880 tubs of Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub, distributed in Illinois. The product contains undeclared egg. Consumers should not consume it and should contact House of Flavors for refund or replacement via email.
GM recalls 2025 Chevrolet Equinox EV AWD due to brake software that may not engage braking as expected. Dealers will update the brake system control module software at no charge. Owner letters mailed Feb. 13, 2025. GM contact: 1-800-222-1020. NHTSA recall number 25V012000.
Zarlengo Italian Ice recalled 757 units of chocolate gelato across multiple sizes in Illinois, Indiana and Texas. The issue centers on a soy lecithin omission in the contains statement. Consumers should not eat the product and should seek a refund or replacement.
Fourour Kiddies recalled tip restraint kits after tests found plastic components could break, creating a tip-over risk. The recall affects kits used to secure furniture to walls. Consumers should stop using the recalled restraints and seek a stainless steel replacement from 4our Kiddies.
Bioenrrty recalled MPINOI branded adult portable bed rails sold on Amazon after reports of serious entrapment and potential asphyxiation. The recall cites a violation of a mandatory standard and missing hazard warnings. Consumers should stop using the product immediately and seek a full refund.
Fagron Compounding Services is recalling 11,680 bags of Vancomycin HCl 1 g in 250 mL 0.9% Sodium Chloride Injection. The recall is nationwide in the United States. The blue break-off part could detach from the administration port, raising sterility concerns. Stop using immediately and contact the provider for guidance.
Riverence Provisions LLC recalls 3,672 units of Smoked Trout Dip sold frozen in cases distributed to eight states over milk allergen labeling. The recall is active as of April 15, 2026. Do not consume the product. Contact Riverence Provisions for refund or replacement.
Honda recalls 2023-2025 Pilot and 2023-2024 Passport vehicles due to potential fuel filler neck tube and pipe separation. The defect can allow fuel leaks with a fire risk. Owners should contact Honda for inspection and repair at no cost. Recall OKM is in effect; letters mailed January 7, 2025.
Siemens Medical Solutions USA recalled 758 units in the U.S. and 2,077 outside the U.S. of ARTIS pheno and ARTIS Icono imaging systems after a dose-display anomaly could misrepresent high X-ray doses. The devices may still be within regulatory dose limits, but the displayed dose may appear significantly higher. Clinicians should stop using the devices and await manufacturer guidance.
Philips Medical Systems Nederland B.V. recalled 3,552 Vue Motion V12 devices worldwide, including the United States. The recall is due to a potential that mis-ordered frames during dynamic cine runs may display out of sequence. Stop using the device and follow the recall instructions provided by the manufacturer.
Cook Medical recalled 20 arterial pressure monitoring trays worldwide after labeling showed expiration dates that exceeded true shelf life. The recall targets two reference part numbers, APMY-2.5-15-0-2.5 and APMY-4.0-21J-1-12. Healthcare providers should stop using affected lots immediately and follow recall instructions.
Cook Medical recalled 5,080 Spectrum Central Venous Catheter Sets worldwide after labeling that indicated expiration dates beyond the products' true shelf life. The recall alerts patients and healthcare providers to stop using affected lots and follow manufacturer instructions.
Cook Medical recalled 15 CTO-6 Micro Wire Guides sold worldwide after labeling errors extended expiration dates beyond true shelf life. The devices carry Reference Part Number CMW-14-190-6G and Order Number G50786. Healthcare providers were notified to stop use immediately until further instructions.
Cook Medical recalled 916 units of the Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set worldwide after discovering expiration dates exceeded true shelf life. The recall affects multiple reference part numbers and order numbers. Healthcare providers should stop using the device immediately and follow Cook’s instructions for recall notification.
Cook Incorporated recalls 484 Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Sets due to expiration date labeling that exceeds true shelf life. The recall is active and distributed worldwide. Health care providers must stop use and follow recall instructions.
Cook Medical recalled 70 NCompass nitinol stone extractors worldwide after labeling showed expiration dates that exceed their true shelf life. The recall affects lots labeled C-NTSE-2.4-115-NC3 (G36250) and C-NTSE-2.4-115-NCT4 (G36251). The company classifies the action as Class II and says the issue could affect patient safety.
Cook Medical issued a global recall of 95 units of the Cook Staged Extubation Set due to expiration dates that exceed true shelf life. The affected lots carry Reference Part Number C-CAE-14.0-83-EXTU and Order Number G24073. The recall is classified as HIGH hazard. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Cook Incorporated.
Toyota recalls 2022-2025 Tundra and Tundra Hybrid vehicles because moisture in the reverse light assemblies can cause light failure. Dealers will replace both reverse light assemblies and repair wire harnesses. Owner letters were mailed September 11, 2025. Contact Toyota at 1-800-331-4331 for recall 24TB06 and 24TA06.