794 recalls tagged with “infant product”.
Straumann USA recalled 61 Emdogain demonstration devices distributed nationwide in 10 states. The devices, intended for demonstration only, could be placed in patients. Healthcare providers and patients should stop using immediately and follow recall instructions from Straumann for disposal or replacement.
M.C.I. Foods recalled 330 cases of Cheese and Egg with Green Salsa Breakfast Burrito sold to seven distributors nationwide. The ready-to-eat burrito contains a cooked egg ingredient that tested positive for Listeria monocytogenes. Consumers should not eat the product and should contact M.C.I. Foods for refund or replacement by letter.
Yamaha recalled model year 2017-2024 DR2A and DR2E Personal Transportation Vehicles sold through Yamaha dealers nationwide from June 2018 through July 2025. The brake system may fail to engage, creating a crash hazard with potential for serious injury or death. Owners should stop using the recalled golf cars and contact an authorized Yamaha Golf Car dealer to arrange a free brake repair. Yamaha or
WLIVE recalled its Fabric 12-Drawer Dressers sold on Amazon after identifying a serious tip-over and entrapment hazard. The dressers are unstable if not anchored to the wall, violating the mandatory standard for clothing storage units under the STURDY Act. Consumers should stop using the recalled dressers immediately and contact WLIVE for a full refund.
RH recalled Byron tables and desks sold at RH Galleries and outlets and on RH.com from November 2023 through July 2025. The recall covers 31 SKUs across three models with stone and marble tops and wood legs. The recalled furniture can collapse if a gap forms between the leg and tabletop and a horizontal force is applied. Consumers should stop using recalled units and contact RH for a full refund,,
AOWOS recalled approximately 42,000 12-drawer dressers sold on Walmart.com due to a tip-over hazard. The dressers lack stability if not anchored to the wall, posing serious risks of injury or death to children. Consumers should stop using the dressers immediately and contact AOWOS for a full refund.
M.C.I. Foods recalled 1,040 cases of ready-to-eat Egg and Cheese Breakfast Burritos and Wraps sold to seven distributors nationwide for institutional use. A cooked egg ingredient used in the ready-to-eat products tested positive for Listeria monocytogenes. Consumers should not consume the product and should contact M.C.I. Foods for refund or replacement; notification will be by letter.
Belivium recalled its baby loungers sold on Amazon after safety concerns tied to suffocation and entrapment hazards. The loungers have a foam sleeping pad and padded bumpers with a cloth cover. Parents should stop using the loungers immediately and contact Belivium for a full refund.
DermaSensor recalled 343 units of its DermaSensor 10101 diagnostic device distributed to medical practices across several states. The device may not meet specifications, producing incorrect results or delaying referrals for patients with suspicious skin lesions. Health care providers should stop using the device immediately and contact Dermasensor Inc for instructions.
CA Botana International recalls Sunscreen Flawless Skin Fluid Tint SPF 50 after CGMP deviations. The recall covers 1,401 tubes distributed to California, Colorado, Florida, Puerto Rico and Washington. Stop using the product and contact CA Botana for guidance.
CA Botana International recalled 1,167 tubes of Doctor. D. Schwab Mineral Sunscreen SPF 50 after CGMP deviations were found. The recall cover identifies lot D54596 with exp 1/31/2028. The distribution includes California, Colorado, Florida, Puerto Rico and Washington.
CA Botana International recalled 805 tubes of Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30 after CGMP deviations were identified. The recall covers tubes sold in California, Colorado, Florida, Puerto Rico, and Washington. Consumers should stop using the product immediately and contact the company for guidance.
CLEARSTEM You Are Sunshine SPF 50 sunscreen from VISAGE is recalled for CGMP deviations. 4,890 bottles distributed to CA, CO, FL, PR, and WA are affected. Consumers should stop using the product immediately and contact CA Botana International or a healthcare provider for guidance.
Sugared+Bronzed recalled 2,090 tubes of tinted mineral sunscreen distributed to California, Colorado, Florida, Puerto Rico and Washington after CGMP deviations were found. The recall, initiated by CA BOTANA International, is active as of Dec 3, 2025. Consumers should stop using the product immediately and contact the distributor for guidance.
Elixir by Coco March Mineral Sunscreen SPF 50 was recalled on 2025-10-10 and remains active. Manufactured or distributed by CA Botana International and distributed in several states. The FDA recall cites CGMP deviations as the hazard. Consumers and healthcare providers should stop using the product immediately and consult a healthcare provider for guidance.
Gabriel Mineral Sunscreen SPF 50 is recalled. The FDA-listed recall number D-0190-2026 covers 1617 tubes distributed to California, Colorado, Florida, Puerto Rico and Washington. The recall cites CGMP deviations as the hazard. Consumers should stop using the product immediately and contact CA Botana International or a healthcare provider for guidance.
A recall is active for Elixir by Coco March Tinted Mineral Sunscreen SPF 50 amid CGMP deviations. The product is distributed by CA Botana International, Inc. The recall cites CGMP deviations as the hazard and class II designation. Consumers should stop using the product and follow guidance from healthcare providers.
CA BOTANA International recalled 874 tubes of Sea Enzyme Ultra Umbrella Sunscreen SPF 30. The recall, active as of Dec 3, 2025, covers tubes with lot D53950 and expiration 05/31/2027 distributed in CA, CO, FL, PR, and WA. The agency cites CGMP deviations as the hazard. Consumers should stop using this product immediately and contact CA BOTANA for guidance or consult a healthcare provider.
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.
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.