These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
3,609 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Kia America, Inc. recalled certain 2023-2025 Niro EV, PHEV, and Hybrid vehicles due to faulty front passenger seat wiring. This issue may prevent air bags and seat belts from deploying correctly or lead to unintended air bag deployment. Owners must stop using the affected vehicles and contact Kia immediately to arrange for inspections and repairs.
Ford recalls 2025 Explorer and Lincoln Aviator vehicles due to loose transmission cross member bolts. The recall covers 2025 models with a high risk of loss of drive power and potential crashes. Owners should contact Ford at 1-866-436-7332 and refer to recall 25S03 for details.
This recall involves Hepo-branded adult portable bed rails, model 110039. The recalled bed rails have white tubing with black foam rubber handle grips, a black fabric pouch, and measures about 16 inches wide by 25 inches high. The model number is located on the original product packaging.
This recall involves Malker Bicycle Light Sets. The bicycle lights were sold in 4- or 8-pack sizes. The products made with red silicone emit red light, products with black silicone emit white light, and products with white silicone emit white light. Each light contains two preinstalled CR2032 button cell batteries. The bicycle lights have "Malker Bicycle Light" printed on labels located on the front packaging. Recalled Bicycle Light Sets: Pack Description Price 8 Piece 4 pcs red & 4 pcs black 9.99 4 Piece 2 pcs red & 2 pcs black $6.99 4 Piece 2 pcs red & 2 pcs white 6.99 4 Piece 4 pcs black $6.99
This recall involves the bottles of 1-K Kerosene Heater Fuel. The bottles come in transparent plastic containers with white caps and have a multicolor label with "KEROSENE" in all capital white lettering and "1-K HEATER FUEL" in similar lettering. The label only has a single front panel and contains warnings and distributor information.
This recall involves unexpired Travel Size Afrin® Original Nasal Spray 6 mL bottles, with Lot numbers 230361, 240822, 241198, 250066, 250152, 250646, and 250831. These travel size bottles have "Afrin® Original Nasal Spray" and "1/5 FL OZ (6 mL)" printed on a label located on the front of the bottle. It is a six-digit number, followed by the expiration date in following format: "YYYYMMM". No other sizes of Afrin are included in this recall.
This recall involves UHOMEPRO 5-Drawer Dressers. The recalled dressers are made of particle board and were sold in black and white. The dresser has five drawers, each with a golden handle. The dresser is 26 inches long by 15.7 inches wide by 38.6 inches tall and weighs about 66 pounds.
This recall involves model year 2025-2026 Honda off-road motorcycles with model numbers CRF250R/RX/RWE or CRF450R/RX/RWE. The model number can be found on the front of the bike in white letters. The white Honda logo is printed on both sides of the back of the motorcycle. The motorcycles have a red chassis. The vehicle identification number (VIN) can be found on the left side of the steering head on all models. Consumers can check if their VIN is included in the recall at https://powersports.honda.com/recalls.
This recall involves the Heartwarming Hugs weighted plush bear with model number 034464. It has a side pouch containing a heart filled with 2.5 pounds of ceramic beads, which can be heated or cooled for comfort. The pouch is secured with a zipper. The product is graded 3 years+ and carries a cautionary statement advising adult supervision due to the heated/cooled element. The model number is located on the label sewn into the back side of one bear leg.
This recall involves DGIVOVO US-branded pressure washers. The recalled, electric pressure washers are red, green or blue with black, and measure about seven inches high, nine inches wide and eight inches deep. They came with a 500 ml spray can attachment, foam cannon, four connect nozzles, a 20-foot hose and two rollers. "Model: C4012PLUS-1500C" is printed on a label located on the back of the pressure washers.
This recall involves the StrikeLock hoistway door locking device, used to secure a residential elevator hoistway landing door. The product is silver in color. The door locking device is installed into the landing door jamb and looks similar to a standard door latch plate.
This recall involves all Stephan Baby-branded Boo Bunnie and Friends children's toys. The recalled toys consist of a small plush animal with a removable, water-filled plastic cube that can be chilled for comfort. The toys measure between 3.5 and 3.7 inches long, between 2.5 and 3 inches tall and between 2.3 and 2.5 inches wide and were sold in various colors and animal shapes. "Stephan BABY" is printed on a sewn-in label located along the side seam on the right underside of the plush and on the front and on the underside of the toys' box packaging.
This recall involves Qumeney Bicycle Light Sets, models: BL-01 and BL-02. The bicycle lights are encased in silicone material and available in six colors including: black, white, red, green, yellow and blue. They are sold in packs of six (one of each color) and 24 (four of each color), each light contains two button cell batteries. The bicycle lights have "QUMENEY" printed on the labels located at the top of the package.
This recall involves Segmart 4-Drawer Dressers. The recalled dressers are made of particle board and were sold in black and white. The dressers have four drawers, are 15.7 inches long by 26 inches wide by 28.5 inches tall and weigh 70 pounds. Model numbers "FFLWM002BK" or "FFLWM002WE" are printed on labels located the product packaging.
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit