2,153 recalls tagged with “stop use immediately”.
Mom Genius recalled retractable safety gates due to entrapment risk that can cause serious injury or death. The recall covers gates with a retractable mesh screen in black and gray. The model is SH.20.006B02. Consumers should stop using the gate and seek a full refund.
Rong Shing Trading NY Inc recalled Aojia Dried Red Bayberry sold in 5.6-ounce bottles after undeclared sulfites and cyclamates were detected. The recall covers 10 cases distributed to Virginia, New Jersey, Massachusetts and New York. Consumers should not eat the product and should contact Rong Shing Trading NY Inc for a refund or replacement.
Pivotal Health Solutions is recalling 34 Quantum Q400 intersegmental heated massage tables sold nationwide in the United States, Canada and Japan. The recall cites heat-function components that can be damaged over time when pressed, risking overheating, smoldering and melting of the vinyl cushion. Clinicians and patients should stop using the device immediately and await manufacturer instructions.
Generic magnetic ball sets sold on Amazon by Ritons are recalled after a high-risk ingestion hazard was identified. The magnets, 3 mm in size and packed in sets of 1,000, can cause serious injury or death if swallowed. Consumers should stop using the recalled product immediately and contact Ritons for a refund with a prepaid return label.
EcoFlow Technology recalled Delta Max 2000 Model EFD310 portable power stations. The units may overheat and ignite, posing a burn and fire risk. Consumers should stop using the recalled power stations and follow EcoFlow’s instructions to install a firmware update for repair.
ALDI is recalling Ambiano electric pressure cookers sold nationwide. The recall affects models 93550 (KY-318B), 96775 (KY-318A), and 98527 (6L-PC). The recall covers 6-quart and 8-quart units. Stainless front branding and a bottom permanent label show the model numbers. Consumers should stop using the units and seek a refund.
ibspot recalled Taoscare Motion Sickness Patches, 36-count boxes, sold in Wyoming and Virginia. The recall centers on marketing without an approved NDA or ANDA. Consumers and healthcare providers should stop using the product immediately and contact ibspot for guidance.
Living Glow recalled for a fire hazard. Guangzhou Jiguang Lighting manufactured the waist fan sold by HSN from May 2025 through July 2025 for $20-$25. Consumers should immediately stop using the recalled device and register for a full refund.
YGJT recalled baby loungers sold on SHEIN by YGJT Local Warehouse from June 2025 through August 2025 for $18-$21. The recall cites a safety violation that allows infants to be trapped or fall due to low sides, wide openings at the foot, and no stand. Consumers should stop using the loungers immediately and request a full refund by emailing YGJTrecall@outlook.com.
USV Private recalled 8,952 bottles of Olopatadine Hydrochloride Ophthalmic Solution USP 0.1%. The product was distributed nationwide in the United States. The defect is failure of impurities/degradation specifications due to an unspecified impurity exceeding the limit. Stop using immediately and contact USV Private Limited or a healthcare provider for guidance.
Calico Brands recalls the Scripto Premium Torch due to fire and burn hazards. The recall covers torches with a four-position adjustable metal nozzle and a hands-free operation lock. Consumers should stop using the recalled torches and return them to the retailer for a full refund or store credit.
STAQ Pharma recalled FentaNYL Citrate PF IV injection nationwide after labeling left incorrect or missing lot and expiration dates. Healthcare providers must stop using the product immediately. STAQ Pharma will provide recall instructions by letter.
Glycar SA recalls 18 SJM Pericardial Patch with EnCap Technology 5x10 cm distributed in the US to healthcare facilities. The lot may not meet the required tensile strength specification. Stop use and follow manufacturer instructions provided by Glycar and your healthcare provider. Notification was issued by email.
STAQ Pharma’s Hydromorphone HCl PF 10mg/50mL IV injection recall affects nationwide distribution in the United States. The recall cites labeling errors involving incorrect or missing lot and expiration dates. Healthcare providers and patients must stop using the product and follow guidance from STAQ Pharma or their clinician.
STAQ Pharma recalled Ketamine Hydrochloride injections distributed nationwide in the United States. The labeling has incorrect or missing lot and expiration date information. Stop using the product and contact STAQ Pharma or your healthcare provider for guidance.
27,868 blister packs of Sucralfate Tablets, 1 g, distributed nationwide by American Health Packaging are recalled. The recall stems from CGMP deviations that prevent the firm from assuring product identity, strength, quality and purity. Health providers and consumers should stop using the product immediately and await guidance.
AstraZeneca recalls 916 Fasenra benralizumab injections distributed nationwide in the United States. The lot is YJ0152 and the NDC is 0310-1730-30. The product is being recalled for lack of sterility assurance. Stop using this product immediately and contact AstraZeneca for guidance.
Del Mar Food Products Corp. recalls 966 cases of Organic IQF Chopped Spinach 35 lbs sold in the United States, including Minnesota distribution. The product may be contaminated with Listeria monocytogenes. Consumers who purchased the spinach should not eat it and should contact Del Mar Food Products for refund or replacement.
Rising Pharma Holdings recalled 2,064 bottles of Carbidopa, Levodopa and Entacapone tablets distributed nationwide in the United States. Sealed bottles labeled 25 mg/100 mg/200 mg contained 37.5 mg/150 mg/200 mg instead. Healthcare providers and patients should stop using immediately and await recall letter guidance.
Nutrition for Longevity recalled 635 Loaded Veggie Grain Bowls shipped directly to consumers in 11 states after a potential Listeria monocytogenes contamination was identified. The recall involves a 309 g ready-to-eat veggie bowl with N4L code V3FR and model 25254. Consumers should stop using the product and contact Nutrition for Longevity for refund or replacement.