2,679 recalls tagged with “immediate action”.
Apollo recalled 2,000 Apollo City 2024 electric scooters sold by Apollo. A weld-line crack can cause the stem to break, creating fall and injury hazards. Owners should stop riding immediately and contact Apollo for a free stem replacement.
Pura Scents recalled the Pura 4 Smart Home Fragrance Diffusers sold at retailers on July 24, 2025. The detachable cover contains five magnets and can detach, creating an ingestion hazard for children. Consumers should stop using the diffuser immediately and contact Pura Scents for a free replacement front cover.
Cipla USA Inc. recalls 20,352 packs of Albuterol Sulfate Inhalation Aerosol after failing stability specifications. The defective lots were distributed nationwide in the United States. The issue involves out of specification results in particle size distribution at the 12-month time point. Patients and healthcare providers should stop use and contact Cipla USA for guidance.
Hyundai Motor America recalls 2025 IONIQ 5 vehicles due to a potentially loose bus bar in the high voltage battery system. The recall covers 2025 IONIQ 5 models. Hyundai says a short circuit could cause a fire. Owners should park outside away from structures until the remedy is complete and contact Hyundai at 1-855-371-9460. The recall number is 280.
Curtis International Ltd. recalled Frigidaire-brand minifridges sold nationwide after more than $700,000 in property damage was reported. Internal electrical components can short circuit and ignite the surrounding plastic housing. Consumers should stop using recalled units immediately and contact Curtis for a full refund.
FENGQS recalled F7 Pro electric bikes with batteries produced on 2024-04-21. The bikes were sold blue and marketed under the FENGQS name. The lithium-ion battery can overheat and ignite, creating a fire and burn risk. Consumers should stop using the recalled bikes immediately and contact FENGQS for a full refund.
Minongad recalled LED Gloves model ST01 after safety violations exposed battery ingestion risk. The recall covers gloves sold on Amazon with two pre-installed lithium coin batteries and four spare batteries. Consumers should stop using the gloves immediately and return them for a full refund.
Beckman Coulter recalled 685 boxes of MicroScan Neg MIC 56 panels distributed nationwide to U.S. healthcare facilities after contamination was reported in wells. Contamination could lead to unreliable antimicrobial susceptibility and organism-identification results. Health care providers should stop using the panels and follow Beckman Coulter recall instructions immediately.
BMW of North America recalls 2022–2025 i4, 2022–2024 iX, 2023–2024 i7, and 2024 i5 vehicles over software that may shut down the high-voltage system, causing loss of drive power. OTA software updates or dealer service will fix the issue at no cost. Letters to owners begin August 5, 2025.
Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes for external use. The U.S. FDA listing cites lack of assurance of sterility as the reason for recall. Consumers and healthcare providers should stop using this product immediately and contact the manufacturer for guidance.
Bestway, Intex and Polygroup recall 5 million above-ground pools taller than 48 inches after nine deaths. The recall covers pools whose model numbers are printed on the liner outside the pool. The hazard stems from a compression strap around the pool legs that can create a foothold for a child, enabling access to the water. Stop using the pools immediately and contact the respective brands for a维修
Middlefield Original Cheese Cooperative recalled 640 pounds of cheese products due to potential Listeria monocytogenes contamination. The recall covers Monterey Jack and Farmers Cheese in multiple package sizes. Consumers should not eat the cheese and should contact the company for refunds or replacements.
Middlefield Original Cheese Cooperative recalled Pepper Jack cheese products sold in Kentucky, Ohio and Pennsylvania after diet contamination concerns. The recall covers 8 oz. individual units, 5 lb loaves and 40 lb loaves with lot code 251661. The hazard is possible contamination with Listeria monocytogenes. Consumers should not eat the product and should contact the company for refund or a safe-
Merck Sharp & Dohme LLC recalled 51,320 cartons of Belsomra (suvorexant) tablets after identifying a risk of delayed dissolution. This defect can delay the release of the drug, hindering sleep onset. Consumers and healthcare providers should stop using the product immediately and contact the company for guidance.
A high-hazard recall is active for Quick Touch Alcohol Prep Pads. 500 cases are affected. The recall covers products from YANGZHOU YULOU PAPER PRODUCTS CO. and AUM Pharmaceuticals. Consumers should stop using immediately and consult healthcare providers for guidance.
Ascend Laboratories recalls 8,568 bottles of Amlodipine and Olmesartan Medoxomil tablets due to failed dissolution specifications. The recall covers products manufactured by Alkem Laboratories in India and distributed nationwide in the USA. The defect involves low dissolution results. Stop use immediately and contact Ascend Laboratories for guidance.
Summa Therapeutics recalled 22 units of the Finesse BTK Multicath Injectable Angioplasty Balloon Catheter sold to healthcare facilities in New Jersey and Florida. The balloon may not meet burst specifications, raising risk during angioplasty. Healthcare providers must stop using the device immediately and follow recall instructions from Summa Therapeutics.
DJO Surgical recalled 907 units of the ALTIVATE reverse wedge glenoid reamer boss drill 6.5mm sold nationwide in the United States. The device may kick or bind up during use. Healthcare providers and patients should stop using the device immediately and follow recall instructions from Encore Medical, LP.
DJO Surgical recalled 927 ALTIVATE reverse wedge glenoid reamer heads distributed nationwide in the United States after concerns that the devices may kick or bind up during use. The issue involves model 804-06-311 and non-sterile stainless steel material. Healthcare providers and patients should stop using the device immediately and contact Encore Medical, LP for instructions.
DJO Surgical is recalling 447 ALTIVATE Reverse Glenoid Reamer Sleeve devices distributed nationwide in the United States. The device may kick or bind up during or immediately prior to use. Healthcare providers and patients should stop using the device and follow recall instructions issued by Encore Medical, LP via email.