2,679 recalls tagged with “immediate action”.
WLIVE recalled its Fabric 15-Drawer Dressers sold on Amazon after reports of tip-over and entrapment hazards. The dressers can tip when not anchored to a wall, posing serious injury or death risk to children and violating the STURDY standard. Consumers should stop using unanchored dressers and contact WLIVE for a full refund.
Boothwyn Pharmacy LLC issued a nationwide recall of 186 vials of Semaglutide 2.5 mg/mL injection, 0.8 mL, on July 9, 2025. The FDA enforcement report classifies the recall as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and follow guidance from Boothwyn Pharmacy or a healthcare provider.
Boothwyn Pharmacy recalls 642 vials of semaglutide 2.5 mg/mL injection sold nationwide in the U.S. The recall cites subpotent drug with Class II designation. Consumers and healthcare providers should stop using the product immediately and contact Boothwyn Pharmacy for guidance.
Boothwyn Pharmacy recalls 8 vials of Fluorescein 2% Ophth 3 mL nationwide after a subpotent drug finding. The recall was issued July 9, 2025 and remains active.
Boothwyn Pharmacy recalls 648 vials of semaglutide 2.5 mg/mL injection nationwide after detecting subpotent potency. The recall involves products distributed across the U.S. and is classified as Class II with a high hazard level. Stop using the product and contact Boothwyn Pharmacy or a healthcare provider for guidance.
Boston Scientific Neuromodulation recalls 25,260 Vercise DBS devices worldwide over wire breaks in rechargeable implantable pulse generators. The defect can prevent stimulation and trigger device removal. Patients should contact their provider for guidance and stop using affected devices immediately.
H-E-B and its inControl brand recall 300,000 sterile alcohol pads nationwide after the FDA alerted a subpotent isopropyl alcohol concentration. The pads were packaged in China with components from Taiwan and distributed nationwide. Consumers should stop using the product immediately and seek guidance from healthcare providers or MEDLINE INDUSTRIES, LP.
Walmart’s ReliOn sterile alcohol swabs are recalled nationwide due to subpotent isopropyl alcohol. The FDA notice lists 3,456,000 pads affected across 4,800 per case and 24 boxes per case. Consumers should stop use and contact Medline Industries or a healthcare provider for guidance.
Medline Industries recalled 6,669,874 units of Alcohol Prep Pads nationwide after detecting subpotent isopropyl alcohol. The pads were distributed nationwide. The recall is classified as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and contact Medline for guidance.
Rite Aid alcohol prep pads distributed nationwide are recalled after subpotent isopropyl alcohol levels were found below label concentration. Medline Industries, LP notified distributors and healthcare providers in a Class II recall dated July 7, 2025. Consumers and healthcare providers should stop using the product immediately and seek guidance from a healthcare provider.
Good Neighbor Pharmacy recalled 66,000 alcohol prep pads for subpotent isopropyl alcohol levels. The pads do not meet the labeled concentration, posing a risk to users. Consumers should stop using the pads immediately and consult their healthcare provider for guidance.
Evergreen Orchard Farm recalled 78 cases of Grape Juice in 4 oz foil pouches distributed to PA, NJ and NY. The recall cites lack of pasteurization and sanitation records. Consumers who purchased the product should not consume it and should contact Evergreen Orchard Farm, LLC via Email for refund or replacement.
Evergreen Orchard Farm recalled 197 cases of Jujube Juice on July 3, 2025, due to lack of pasteurization and sanitation records. This oversight poses a significant health risk from potential contamination. Consumers should not consume the product and contact Evergreen Orchard Farm for a full refund.
Evergreen Orchard Farm recalled 610 cases of Korean Pear Juice distributed in Pennsylvania, New Jersey and New York after finding a lack of pasteurization and sanitation records. The recall highlights a potential adulteration risk. Consumers who purchased this product should not drink it and should contact Evergreen Orchard Farm for refunds or replacements via email.
Tandem Diabetes Care recalls 19 units of the t:slim X2 insulin pump with interoperable technology distributed internationally, including Israel. An app defect occurs when the phone uses a right-to-left language and can cause app-pump pairing problems and graphical defects. Patients should stop using the device immediately and follow the manufacturer’s recall instructions.
North American Rescue recalled 552 units of the JETT device, used for occlusion of blood flow to the lower limbs, due to a manufacturing defect that may compromise structural integrity and performance. The recall covers multiple kits distributed worldwide, including U.S. states and several international countries. Stop using the device immediately and await recall instructions from the company or
Honda recalls 2025 CR-V Hybrid vehicles sold through Honda dealers nationwide after finding an improperly installed fuel feed hose that may leak. The recall is identified by Honda as TLS. Dealers will replace the fuel feed hose and install a new connector cover at no charge. Owners should contact Honda at 1-888-234-2138 for service.
Volkswagen Group of America recalls 2023-2025 Atlas, Atlas Cross Sport and 2023-2024 ID.4 models for loose bolts in the chassis, brake system and suspension. The potential consequence is loss of vehicle control and a crash risk. Owners should stop driving the vehicle and contact a dealer for inspection; recall letters were mailed on July 25, 2025.
CHETAK NEW YORK LLC recalled 5,232 packets of Deep Sprouted Mat 16 oz distributed to California, New Jersey, Illinois, Florida and Texas after tests found Salmonella. The recall class is I with a high hazard level. Consumers should not consume the product and should seek refund or replacement by email.
Ford Motor Company recalls certain 2025 Expedition and Navigator vehicles due to a passenger-side frontal air bag that may deploy with excessive force. Dealers will replace the passenger side air bags at no charge. Owner notification letters were mailed August 8, 2025.