Every parent needs to see this: 353 high-risk children's product recalls currently active. Check your home now.
386 baby and children's product recalls tracked. Protect your kids from dangerous toys, cribs, car seats, furniture, and other hazardous products.
Every year, emergency rooms treat approximately 150,000 children under age 15 for toy-related injuries, according to the Consumer Product Safety Commission (CPSC). Many of these injuries could be prevented with better awareness of product recalls and safety standards.
Children are uniquely vulnerable to product hazards because they explore the world by touching, tasting, and testing everything around them. Products designed for adults may pose unexpected risks when children gain access to them, and even products specifically made for children can have manufacturing defects or design flaws.
Staying informed about recalls is one of the most effective ways to protect your children. When a recall is announced, the manufacturer has determined (or a government agency has found) that the product poses a genuine safety risk that warrants action.
Help other parents: Share this page with parent groups, playdate friends, and family members. Every parent deserves to know about these safety alerts.
Youbeien recalled crib mobiles after multiple reports of battery ingestion risks. The mobiles can operate without a remote, but the battery compartment in the remote is easily accessible. Consumers should stop using the product and contact GKKBSJ for a full refund immediately.
Goyal Group Inc. recalled 293 sets of SILVER HORSE aluminum cookware, including a 4-inch milk pan and a 26-inch mathar kadai, distributed to customers in multiple states. The FDA enforcement report notes elevated lead levels in the products. Consumers should stop using the cookware and contact Goyal Group for a refund or replacement.
Cardinal Health 200, LLC recalled Salem Sump gastroduodenal tubes worldwide after reports of anti-reflux valve breakage. The ARV can fail under excessive force during use. Healthcare providers and patients should stop using the device immediately and follow the manufacturer instructions for recall communication.
Taproom Gourmet brand bulk Broadway Mix recall covers 3,547 cases distributed across six states. The recall cites no ingredient label and undeclared allergens including peanuts, sesame, wheat and soy. Consumers should not consume the product and should seek refund or replacement through Egress Capital Partners Inc.
D & M Smoked Fish, Inc. recalls 2,022 Haifa Cold Smoked Salmon, 8 oz packages distributed in NY, NJ, PA, WA, CA, IL and FL after Listeria monocytogenes was detected. The recall is classified as high risk. Consumers who bought this product should not eat it and should contact D & M Smoked Fish for a refund or replacement.
Percussionaire recalled 59,160 Phasitron 5 IPV In-Line Valve sets worldwide after an IFU update flagged a pressure-relief leak when used with ventilators. The defect endangers neonates and infants and patients under 10 kg with tidal volumes under 50 mL. Healthcare providers should halt use immediately.
Sprout Organics recalled 9,873 cases of 6+ Months Made With Organic Sweet Potato, Apple & Spinach baby food nationwide. A potential contamination with lead has been identified. Consumers who purchased the product should stop using it and contact Sprout Organics for refund or replacement through the recall notice.
Private Label Skin Care Inc. recalled edunn clarity BP Treatment Cleanser 10% after benzene was detected. The recall covers lot numbers 58170A and 58172A with expiration September 2025. The product was distributed in California and Georgia.
GE HealthCare recalled 1,386 Millennium MG/MC dual-head gamma cameras used in cardiac imaging worldwide. The recall notes devices past End of Guaranteed Service may have been transported without adequate detector support, risking mounting failure and possible detector falls. Facilities should stop using the devices and await recall instructions sent by GE Medical Systems Israel, Functional Imaging
9,936 bottles of Cetirizine Hydrochloride Tablets USP 10 mg were recalled nationwide in the United States. Manufactured by Unique Pharmaceuticals Labs and distributed by Rising Pharma Holdings, the lot carries imprint with the wrong ID. Stop using the product immediately and contact the manufacturer or your healthcare provider for guidance.
M.O.M Enterprises recalled 46,752 bottles of Organic BABY bedtime drops sold nationwide through Unknown retailers after FDA enforcement notice flagged potential yeast contamination. The product is a liquid dietary supplement for infants age 4 months and older. Parents should stop using the product immediately and contact M.O.M Enterprises for refund or replacement.
In My Jammers recalls children's button-up flare pajama sets sold online after the company violated mandatory flammability standards. The recall, active as of Sept. 11, 2025, involves sets in multiple prints and sizes. Parents should stop using them and seek a full refund or store credit.
Shierdu recalled a 28-piece wooden cactus toy set sold on Amazon by Yiwu Shiyi Trading after reports the parts pose a choking hazard for children under three. The recall cites violation of the Small Parts Ban. Parents should stop using the product and contact the supplier for a full refund.
Harris Teeter recalls 295 units of Asiago Texas Toast distributed in eight states after discovering undeclared milk. The allergen milk was not listed in the ingredient statement. Consumers with milk allergies should avoid the product and seek refunds or replacements.
CareFusion 303 BD Alaris infusion pump modules and compatible infusion sets are recalled nationwide in the U.S. and multiple international markets. The recall covers reference numbers including C24101E and 10015414 and related SmartSite components. The defect may cause flow rate and bolus accuracy deviations, and incorrect occlusion timing. Stop using the device and follow recall instructions from
Gina Marie Bakery LLC recalled 172 cases of Italian Sesame Cookies after discovering undeclared sesame and artificial colorings. The recall began with CT state actions and was notified to FDA on 09/10/2025 with customer notification on 09/11/2025. Consumers should not eat these cookies and should seek refunds or replacements.
Goot Essa recalled 62 lbs of Der Mutterschaf Cheese, Sheep Tomme Style, produced in batch #33 at plant #26476, with exp. 12/24/2025. The recall is active after a positive Listeria monocytogenes test. Consumers should not consume this cheese and should contact the company for refund or replacement.
Whole Foods Market recalled 6-pack granola sold at one Philadelphia store after undeclared wheat, sesame and cashew were found. The product was labeled incorrectly. Consumers should not eat the product and should seek refund or replacement from WFM Purchasing, LP.
Lee K of NY Inc. recalls 43 units of PINOCCHIO CATERING Aged Kimchi Mackerel sold in New York and New Jersey for undeclared milk and shrimp. The recall is Class I with a high hazard. Consumers should not consume the product and should contact the company for refunds or replacements.
GE Medical Systems recalled 7,302 AW Server models worldwide, including 1,381 units in the U.S., after identifying a security vulnerability that could expose patient data. The defect could allow a malicious actor to compromise confidentiality, integrity and availability of information. Healthcare providers should stop using the devices immediately and follow manufacturer instructions for recall.
Spacelabs Healthcare recalls 8,179 DVI display cables worldwide after EMI interference could affect medical monitors. The cables connect 6-foot DVI-I to DVI-I devices used with the 91390 and 91393 monitors. Healthcare providers should stop using affected cables and follow recall instructions.
URMYWO recalled its baby loungers on 2025-09-04 after reports of suffocation and fall hazards. The recall targets URMYWO loungers style grey feather sold via Amazon by Pomona. The devices fail to meet infant sleep standards due to short side walls and excessive pad thickness. Consumers should stop using the loungers and request a full refund.
Pacific Coast Producers recalled 102 cases of Halved Pears in Pear Juice Concentrate sold nationwide through Wegmans distribution after detecting potential lead contamination. The product is packaged in 15-ounce cans with Lot 6PJ 09 C2295 and UPC 077890747490. Consumers should stop using the product and contact Pacific Coast Producers for refund or replacement.
Endico Potatoes Inc recalled 280 cases of Endico brand Frozen Mixed Vegetables distributed to retailers in New York, New Jersey, Connecticut, Florida, Pennsylvania, Maryland and the District of Columbia. The product may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact Endico Potatoes for refunds or replacements.
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