794 recalls tagged with “infant product”.
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.
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.
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.
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.
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.
Sno Pac Foods recalled 4,006 cases of Frozen Organic Spinach sold under Sno Pac Frozen Vegetables and Maika'i Keep Frozen. The spinach may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact Sno Pac Foods for refund or replacement.
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 Inc recalls 4,298 cases of pizza-style shredded cheese blends sold through retailers nationwide after metal fragments were found in supplier raw material. The defect involves potential metal fragments that could contaminate the cheese. Consumers who may own any of the affected products should not consume them and should contact Great Lakes Cheese Co for refund or replacement.
In Motion Design recalled Evermore Surprise Eggs due to lead content above federal limits. The recalled eggs were sold with yellow, pink or green wrap and include a gold egg containing seven toys, including a toy airplane. Consumers should stop using the product and return it for a full refund.
Blossom recalled two-piece children’s loungewear sets sold under its brand due to a burn risk that violates the mandatory flammability standard for children's sleepwear. The recall covers sets in multiple colors and designs sold for sizes 12 months through 12 years. Stop using the garments and contact Blossom for a full refund.
Almpal recalls its dissolved oxygen test kits sold on Amazon after authorities found the sulfuric acid inside the kit lacked required child-resistant packaging. The recall is active as of Oct 2, 2025. Consumers should stop using the kit and follow disposal and refund instructions from the seller.
Zyntony recalled Kogalla power banks sold on Kogalla.com due to fire and burn hazards. The recall targets BP125, BatPak 2F and BatPak 3F models. The lithium-ion batteries can overheat and ignite, even when not in use. Consumers should stop using the recalled power banks and contact Kogalla for a free replacement.
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.
Church & Dwight recalled 21,912 bottles of ZICAM Cold Remedy Medicated Fruit Drops Elderberry from nationwide distribution in the United States. The label did not indicate elderberry as an ingredient though the product contains elderberry. Consumers should stop using the product and contact Church & Dwight for guidance.
Camber Pharmaceuticals recalled Ketorolac Tromethamine Injection, USP, 60 mg/2 mL, 2 mL single-dose vials distributed nationwide in the United States. The recall is due to the presence of glass particulates. Healthcare providers and patients should stop using the product immediately and contact Aspiro Pharma Limited at 1-866-495-1995 for guidance.
Abiomed recalled 10,153 Automated Impella Controllers and related components due to potential cybersecurity vulnerabilities in the operating system. The recall spans multiple international product codes and was first issued for devices distributed nationwide and internationally. Providers should stop using the affected controllers and follow manufacturer instructions immediately.
Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider 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.
Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 interventional fluoroscopic x-ray systems distributed in 14 countries. The defect is corrosion of the IITV control board that may cause loss of imaging functionality or poor image quality. Healthcare providers and patients should stop using the device and follow manufacturer instructions for recall remediation.
Vicky IT recalled 10 pounds of Bona Fish distributed in New York after FDA enforcement flagged the product for serious safety hazards. The recall cites un-eviscerated fish that may be contaminated with Clostridia botulinum, along with mold and insect larvae. Consumers who bought Bona Fish should not consume it and should contact Vicky IT for a refund or replacement.