2,153 recalls tagged with “stop use immediately”.
123Herbals LLC recalled SILINTAN 25-pill bottles sold nationwide in the United States after FDA analysis found undeclared meloxicam. An NDA/ANDA violation is cited. Consumers and healthcare providers should stop using this product immediately and contact 123Herbals LLC for guidance.
Town Food Service EQ CO Inc. recalled approximately 11,300 aluminum sauce pans on October 17, 2025, due to leachable lead levels. Consumers should not use these pans and should seek refunds or replacements. The recall affects various sizes sold across multiple states and locations in Canada.
Straumann USA recalled 61 Emdogain demonstration devices distributed nationwide in 10 states. The devices, intended for demonstration only, could be placed in patients. Healthcare providers and patients should stop using immediately and follow recall instructions from Straumann for disposal or replacement.
Nat's Nuts LLC recalled 600 units of Cinnamon Whiskey Pecans sold through multiple retailers. The recall is due to undeclared cashews, creating an allergy risk. Stop using the product and contact Nat's Nuts LLC for refund or replacement information.
WLIVE recalled its Fabric 12-Drawer Dressers sold on Amazon after identifying a serious tip-over and entrapment hazard. The dressers are unstable if not anchored to the wall, violating the mandatory standard for clothing storage units under the STURDY Act. Consumers should stop using the recalled dressers immediately and contact WLIVE for a full refund.
AOWOS recalled approximately 42,000 12-drawer dressers sold on Walmart.com due to a tip-over hazard. The dressers lack stability if not anchored to the wall, posing serious risks of injury or death to children. Consumers should stop using the dressers immediately and contact AOWOS for a full refund.
Super Wheels Inc. recalled Vaast A/1 bicycles and framesets sold through retailers after a fall risk was identified. The frame can develop a hairline fracture near a weld, which can cause the tubes to separate. Owners should stop riding immediately and contact Super Wheels for a free replacement frame and up to $200 for a bike-shop rebuild.
DEVI brand Cinnamon Powder, imported and distributed by Homeneeds Inc. in Bellevue, WA, is recalled after FDA testing found lead at 2.92 mg/kg. The recall covers 7 cases and about 140 packets. Consumers should not consume the product and contact Homeneeds for a refund or replacement.
Yamaha recalls 2021-2025 Drive 2 PTV golf cars sold by Yamaha dealers nationwide between June 2020 and July 2025. The recalled golf cars lack stop lights, creating a crash hazard that could result in serious injury or death. Owners should stop using the recalled golf car immediately and contact an authorized Yamaha Golf Car dealer for a free installation of two stoplights.
Yamaha recalled model year 2017-2024 DR2A and DR2E Personal Transportation Vehicles sold through Yamaha dealers nationwide from June 2018 through July 2025. The brake system may fail to engage, creating a crash hazard with potential for serious injury or death. Owners should stop using the recalled golf cars and contact an authorized Yamaha Golf Car dealer to arrange a free brake repair. Yamaha or
VESTA.DS recalled VST-brand residential tankless water heaters sold nationwide through retailers after the potential carbon monoxide poisoning hazard was identified. The exhaust duct can crack, letting gases escape into homes and potentially cause death or serious injury. Stop using the recalled water heater and contact VESTA.DS for a free repair; if you must continue using it, install working烟雾与一
RH recalled Byron tables and desks sold at RH Galleries and outlets and on RH.com from November 2023 through July 2025. The recall covers 31 SKUs across three models with stone and marble tops and wood legs. The recalled furniture can collapse if a gap forms between the leg and tabletop and a horizontal force is applied. Consumers should stop using recalled units and contact RH for a full refund,,
Belivium recalled its baby loungers sold on Amazon after safety concerns tied to suffocation and entrapment hazards. The loungers have a foam sleeping pad and padded bumpers with a cloth cover. Parents should stop using the loungers immediately and contact Belivium for a full refund.
Wilteexs recall 1-liter bioethanol fuel bottles imported by Wilteexs after safety-standard violations. The bottles lack flame mitigation devices and carry a false “Non Toxic” disclaimer. Consumers should stop using the recalled bottles and contact Wilteexs for a full refund.
M.C.I. Foods recalled 330 cases of Cheese and Egg with Green Salsa Breakfast Burrito sold to seven distributors nationwide. The ready-to-eat burrito contains a cooked egg ingredient that tested positive for Listeria monocytogenes. Consumers should not eat the product and should contact M.C.I. Foods for refund or replacement by letter.
M.C.I. Foods recalled 1,040 cases of ready-to-eat Egg and Cheese Breakfast Burritos and Wraps sold to seven distributors nationwide for institutional use. A cooked egg ingredient used in the ready-to-eat products tested positive for Listeria monocytogenes. Consumers should not consume the product and should contact M.C.I. Foods for refund or replacement; notification will be by letter.
Meadowgold Dairies Hawaii recalled 75,566 half-pint cartons of fat-free chocolate milk distributed in Hawaii. The recall is due to potential quality-control issues. Consumers should not drink the product and should contact Meadowgold Dairies Hawaii LLC for refund or replacement information.
Paragon 28 recalled 20 Phantom Fibula Nails nationwide after finding out-of-spec thread depths. The defect may prevent the nail from mating properly with the mounting bolt. Surgery could be aborted if the implant cannot mate with instrumentation. Hospitals and surgeons should stop using the device immediately and follow recall instructions.
MRIMed recalled 314 batteries for the SL-110 Mobile Exam Light on October 13, 2025. The batteries can overheat while charging, melting internal components and producing smoke. This recall affects devices distributed in the U.S. and several countries worldwide.
DermaSensor recalled 343 units of its DermaSensor 10101 diagnostic device distributed to medical practices across several states. The device may not meet specifications, producing incorrect results or delaying referrals for patients with suspicious skin lesions. Health care providers should stop using the device immediately and contact Dermasensor Inc for instructions.