1,215 recalls tagged with “replacement available”.
PNW Components recalled its Loam Pedal Gen 2 on January 9, 2026, after reports of axle cracks. The defect can cause pedals to detach, posing a fall risk. Customers should stop using the pedals immediately and seek replacements.
Volkswagen recalled 2025 Tiguan vehicles after a rear tie rod bolt may loosen, risking loss of vehicle control. Dealers will replace the bolt at no charge under recall 42E7. Letters were mailed Sept. 5, 2025.
Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.
Ford is recalling certain 2020-2025 Explorer and Aviator SUVs because the easy-entry second-row outer seat switch bezel may bind or stick, causing seats to unlatch, fold, or slide unexpectedly while driving. Dealers will inspect the second-row seat switch and replace the bezel around the switch as necessary, free of charge. Owner notification letters were mailed August 7, 2025; Ford can be reached
Ford is recalling 2025 Explorer SUVs, along with 2025 Transit and F-150 vehicles, due to defects in connecting rods and rod bearings. The issue can cause engine damage and failure. Owner notices were mailed August 15, 2025, and Ford recall number is 25S55. Dealers will inspect and replace the engine long block as needed.
Encon Safety Products recalls AQ 120 GFEW Aquarion Preserved Cartridges sold nationwide through multiple retailers. The recall cites cGMP deviations in manufacturing. Stop using the product immediately and follow recall guidance from Encon Safety or your healthcare provider.
Cipla USA, Inc. is recalling 15,221 Lanreotide Acetate Injection syringes nationwide in the United States after detecting particulate matter. The defect is the presence of particulate matter in the injectable solution. Healthcare providers and patients should stop using the product immediately and contact Cipla USA for guidance.
Toyota recalls 2021-2025 Sienna Hybrid vehicles for third-row seatback bolts that may not be tightened. The unsecured bolts may fail to restrain occupants in a crash. Owners should contact their Toyota dealer for inspection and service; recall number 25TA05; letters were mailed April 1, 2025.
Kia America recalled 2025 Sorento Hybrid and 2024-2025 Sorento SUVs sold at Kia dealerships nationwide after a body domain control software fault may disable low beam headlights and taillights. The defect can reduce visibility and raise crash risk. Owners should contact a Kia dealer for a free software update under recall SC331; notifications were mailed Feb. 21, 2025.
Gold Star Distribution is recalling Tylenol products distributed nationwide. The recall concerns CGMP deviations and insanitary conditions at the distributor’s facility. Consumers should stop using these Tylenol products immediately and contact Gold Star Distribution for guidance.
Gold Star Distribution Inc. is recalling Carmex lip balm in 12-count jars and 12-count tubes distributed nationwide in the United States. The recall cites CGMP deviations and insanitary conditions at the distribution center, including rodent exposure. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution for guidance.
Gold Star Distribution Inc. issued a nationwide recall of Colgate and Crest toothpaste on December 26, 2025 after inspectors found insanitary conditions and rodent exposure at its distribution center. The issue stems from CGMP deviations that could contaminate products. Consumers should stop using the affected toothpaste immediately and contact Gold Star Distribution for guidance.
Gold Star Distribution recalls EXCEDRIN 2'S DISP.- 30 CT distributed nationwide in the United States. The recall cites CGMP deviations due to insanitary conditions including rodent exposure at the distribution center. Consumers and healthcare providers should stop using the product immediately and await guidance from Gold Star Distribution.
Gold Star Distribution recalls Swan White Clear Alcohol, 50% ABV, 16 oz, 12 count, nationwide. FDA enforcement cites CGMP deviations and insanitary distribution-center conditions including rodent exposure. Stop using the product now and contact the distributor or a healthcare provider for guidance.
Bisaf Strep A Self-Test from Altruan GmbH remains active in recall status after the FDA flagged lack of clearance. The Class II medical device was distributed nationwide in the United States. The hazard is lack of FDA clearance. Consumers should stop use immediately and follow manufacturer guidance.
Altruan GmbH recalled 188 units of the Clearest Strep-A Cassette Test distributed nationwide in the United States after determining the device was not cleared by the FDA. The test lacks FDA clearance. Healthcare providers and patients should stop using the test immediately and follow the manufacturer’s recall instructions.
Vascutek recalled 37,430 Gelsoft Plus and Gelweave vascular prostheses distributed nationwide in the United States after discovering the devices were labeled with an extra month of shelf life. The expiry date was calculated from packaging rather than gel impregnation. Healthcare providers and patients should stop using the devices immediately and follow recall instructions.
Prima Vera Nueva recalled 16,790 packages of Black Bean Bonanza Tamales on December 12, 2025. The company cited potential contamination with Listeria monocytogenes, a serious foodborne pathogen. Consumers should not eat these tamales and should seek a refund or replacement.
TREK recalled four electric bicycles sold through Trek authorized retailers and independent bike shops nationwide and online. The chainring bolts can loosen, causing the chainring to detach and create a fall hazard. Owners should stop riding immediately and contact an authorized Trek dealer for a free repair; Trek provides a $20 in-store credit toward Trek, Electra, or Bontrager merchandise, valid
BaoD recalled Uuoeebb Infant Walkers sold on Amazon after safety hazards were identified. The walker can fit through a standard doorway and does not stop at a step edge, creating a fall hazard. The leg openings can allow a child to slip down until the head becomes entrapped. Consumers should stop using the recalled walker immediately and contact BaoD for a full refund.