495 recalls tagged with “suffocation risk”.
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.
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.
Bmrwtg recalled its Children’s LED Tutu Skirts sold on Amazon after battery ingestion safety concerns. The skirts use two CR2032 lithium coin batteries to power the lights. Parents should stop using the recalled skirt immediately and contact Bmrwtg for a full refund.
ESR HaloLock wireless power banks were recalled in an expansion that now includes model 2G505. The recall covers models 2G520, 2G505B and 2G512B previously recalled and adds 2G505. The recall is distributed by Waymeet. The lithium-ion batteries can overheat and ignite. Consumers should stop using recalled power banks and seek a full refund from Waymeet.
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.
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.
Volkswagen Group of America recalls 2025 ID. Buzz vehicles due to an incorrect brake warning light symbol and color on the instrument panel. Dealers will update the instrument panel software at no charge. Letters notifying owners were mailed June 6, 2025. Contact VW at 1-800-893-5298 for recall 90A2.
Great Lakes Cheese Co recalls 4,131 cases of mozzarella and provolone shredded cheese blends sold under four store brands due to metal fragments from supplier raw material. The hazard involves potential metal fragments detected in the shredded cheese products. Consumers should not consume these products and should contact Great Lakes Cheese Co for refund or replacement information.
Coca-Cola Southwest Beverages LLC recalled 2,322 units of Coca-Cola 12oz Can packs sold in Texas. The products include 24-pack and 35-pack configurations with model numbers 49000012781 / JUN2926MAA and 49000058468 / JUN2926MAA. Consumers should not drink these cans and should contact the company for refunds or replacements.
Gunaito recalled 10-drawer dressers sold on Walmart.com after reports of tip-over and entrapment hazards. The recall targets brown and white dressers with model numbers HD006BN-SLCD and HD006WH-SLCD. The product packaging bears the codes HD006BN-SLCD or HD006WH-SLCD.
Amy's Kitchen recalled 38,856 frozen Gluten Free Bean & Rice Burritos across 3,238 cases distributed to 21 states on Oct. 2, 2025. The recall cites potential contamination with foreign objects. Consumers should not eat the product and should contact Amy's Kitchen for refund or replacement information.
ICU Medical recalls 23,203 IV gravity burette sets worldwide. The burette component is missing an internal shutoff valve, which can delay therapy, cause overdelivery, or allow air to be infused. Stop using the device and contact ICU Medical for instructions.
AFCO's hand sanitizer 5515 is being recalled nationwide through distributors and retailers. The recall cites cGMP deviations that left methanol risk unexcluded. Consumers and healthcare providers should stop using this product immediately and contact Acuity Specialty Products for guidance.
Acuity Specialty Products recalled hand sanitizer products sold nationwide due to potential methanol presence. The recall covers Wyandotte, Sanifect E3 ethanol-based sanitizer products manufactured by AFCO. The issue stems from unperformed receipt testing on incoming alcohol components. Consumers and healthcare providers should stop use immediately.
Synthes USA recalled 122 locking intramedullary nail screws used in RFN-Advanced and Tibial Nail Advanced systems. The recall covers worldwide distribution including the US and Canada. The packaging labeling misstates screw length while the etched length on the screw is correct. Healthcare providers should stop using the device immediately and follow recall instructions from Synthes.
Wholesale Produce Supply LLC recalled 307 cases of cantaloupe chunks sold under Fresh & Finest, Harvest Cuts and other labels. The recall targets a broad range of container sizes and UPCs in IA, IL, ND, NE and WI. The recall cites potential Listeria monocytogenes contamination and is classified as Class I.
Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Tray with Strawberries after potential Listeria monocytogenes contamination. The recall covers trays packed in Minneapolis, MN and distributed to Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The product should not be consumed and refunds or replacements are being offered. The recall is active as of the latest notice.
Wegmans Food Markets is recalling 521 units of Wegmans Large Ultimate Plain Cheesecake sold in Virginia, Maryland, North Carolina and Washington D.C. The product contains undeclared pecans. Consumers should stop using the product and contact Wegmans for refund or replacement.
Wholesale Produce Supply LLC DBA recalled 307 cases of Cut Fresh Melon Mix due to potential Listeria monocytogenes contamination. The recall covers multiple Melon Mix products packed by WPS in Minneapolis and distributed to IA, IL, ND, NE, and WI. Consumers should not eat the product and should seek refunds or replacements.
Persilux recalled zebra blinds sold on Amazon after safety hazards were found. The recall cites long operating cords that can cause strangulation and entanglement. The company offers a free repair kit and instructions to remove cords. Consumers should stop using the product immediately and contact Persilux for remedy information.