2,756 recalls tagged with “immediate action”.
Furnulem recalled its five-drawer dressers sold at multiple retailers after safety concerns linked to tip-over and entrapment risks. The dressers can be unstable if not anchored to the wall, posing serious injury or death risk to children. Consumers should stop using the recalled dressers immediately and contact Furnulem for a full refund.
EnHomee recalled its 10-Drawer Dressers sold on Amazon after determining tip-over and entrapment hazards. The recall also notes a violation of the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and contact EnHomee for a full refund.
Clark Associates recalled Lancaster Table & Seating powder-coated aluminum outdoor chairs and barstools in 3 models. The recall covers 180 item numbers and colors across arm chairs, side chairs, and barstools. Consumers should stop using the recalled chairs and contact Clark Associates for a full refund.
Zan International Trading recalls Lotus Joy Organic Sweet Birch Essential Oil bottles due to packaging that is not child-resistant. The product contains methyl salicylate and poses a poisoning risk to children if swallowed. Stop using the product now and return it for a full refund by contacting Zan International Trading.
IF Holding II recalls 1,375 cases of Tippy Toes Apple Pear Banana baby food distributed by Topco Associates LLC in Illinois. The product may contain patulin contamination. Consumers should not consume the product and should contact IF Holding II for a refund or replacement by letter.
Diagnostica Stago recalled 369 STA Liatest Free Protein S kits worldwide on 2026-02-04 due to potential out-of-range results. The defect may underestablish protein S levels in normal plasmas. Stop using immediately and follow the manufacturer’s recall instructions via email.
GE Medical Systems recalled 125 Imactis CT-Navigation System stereotaxic accessories distributed worldwide to healthcare facilities. The recall cites a potential mismatch between the simulated needle trajectory and the actual trajectory. Healthcare providers should stop using the devices immediately and follow the manufacturer's recall instructions.
Mazda North American Operations is recalling certain 2024-2025 CX-50 SUVs equipped with Mazda Genuine Accessory trailer hitches sold through Mazda dealerships. The recall number is 7225C and owner notification letters were mailed April 4, 2025. The recall addresses bolts that may loosen and detach the hitch. Owners should contact their Mazda dealer to schedule a free tightening.
Ford recalls 2024-2025 Explorer and other models for a transmission valve body defect. The valve body may have been machined incorrectly, causing reverse gear failure or unexpected forward movement in reverse or neutral. Owner notification letters were mailed April 11, 2025; dealers will replace the valve body at no charge.
Exactech recalled 120 Equinoxe Ergo Modular Impactor Handles after identifying a missing cross-pin. The defect could compromise instrument integrity during surgical use. Hospitals and surgeons should stop using the devices immediately and follow Exactech's recall instructions.
Ion Beam Applications S.A. recalled four PROTEUS 235 proton therapy systems distributed worldwide, including Florida in the United States, and the countries of Italy and Japan. The defect disables the Therapy Safety System's Universal Beam Triggering Interface, so the system may not stop beam delivery if the Healthy Signal from an external gating device is lost. Patients and healthcare providers应该
Ford Motor Company is recalling 2025 Super Duty F-250, F-350, and F-450 trucks sold through Ford dealers. The steering column shifter may detach due to an improper weld. Owners should stop driving the vehicle and contact a Ford dealer for a free inspection.
Pure Solutions recalled 442 bottles of its sleep supplements on February 3, 2026. The labels did not declare a milk allergen despite containing bovine colostrum. Consumers should stop using the product immediately and seek refunds.
Exactech recalls 596 Equinoxe Core Instrument Kit units due to a missing cross-pin on the impacter handle. The alert, categorized as a Class II recall, was issued Feb 3, 2026 and remains active. Affected kits were distributed across the United States and in multiple international markets. Stop using the device and follow manufacturer instructions for recall remedies.
Prime Food Processing recalled 79 cases of dried croaker fish on February 3, 2026, due to safety concerns. The uneviscerated fish poses a high risk of food poisoning. Consumers should not consume this product and seek refunds.
B. Braun Medical recalled 105,550 BBraun Medical 21G X4.4CM Winged INF devices worldwide, including Texas and Costa Rica. A dull or blunt needle tip may be difficult to advance or break. Healthcare providers and patients should stop using the device and follow the manufacturer's recall instructions.
B. Braun Medical recalls 51,300 units of its 21GA Winged Infusion Set, model 7M2802, distributed worldwide including Texas and Costa Rica. The device’s needle tip can be dull or break, making advancement difficult. Stop using the device immediately and contact the manufacturer or your healthcare provider for instructions.
Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.
Pro Numb Tattoo Numbing Spray was recalled on February 2, 2026 due to cGMP deviations. The product, containing 4% lidocaine, is distributed by Pro Numb Tattoo Numbing Spray LLC. Consumers should stop using it immediately and contact the company for further guidance.
B. Braun Medical is recalling 21,000 21GA Winged Infusion Sets (Single Pack) distributed worldwide, including Texas and Costa Rica, catalog 7A3842. The needle tip can be dull or blunt, may be difficult to advance, or break. Clinicians and patients should stop using the device and await manufacturer instructions.