79 recalls tagged with “mandatory standard violation”.
Furnulem recalled its 8-Drawer Dressers on December 18, 2025, due to tip-over and entrapment hazards. The dressers can cause serious injury or death if not anchored to a wall. Consumers should stop using the product immediately and contact Furnulem for a refund.
Qunol recalled Extra Strength Turmeric Capsules due to mold contamination in raw materials. The recall affects over 3,000 units distributed across 27 states. Consumers should stop use and seek refunds immediately.
Luyuan recalled X-Pro Eagle 40cc and FRP Sahara 40cc Youth ATVs on December 11, 2025. The ATVs violate mandatory safety standards and pose serious injury risks. Consumers must stop using the ATVs and contact Luyuan for a free repair.
Casaottima recalled 50,000 13-drawer dressers on December 4, 2025. The dressers pose a serious risk of tip-over and entrapment hazards to children. Consumers should stop using the dressers immediately if unanchored and seek a refund.
Little Pea Shop recalled crib bumpers on December 4, 2025. The bumpers violate a federal ban and pose a suffocation hazard. Parents should stop using these products immediately.
Lunds & Byerlys recalled 1,296 cookies on December 3, 2025, due to undeclared allergens including peanuts, eggs, and soy. The recall affects 108 cases of Monster Cookies sold in Minnesota. Consumers should not eat the product and seek a refund.
Bosen US recalled Sofoliana and Glotika baby loungers on November 26, 2025. The loungers pose risks of serious injury or death due to entrapment and fall hazards. The product violates mandatory safety standards for infant sleep products.
Vivohome recalled adult portable bed rails on November 26, 2025, due to serious injury hazards. The recalled rails can pose risks of entrapment and asphyxiation. Consumers should stop using them immediately and seek a refund.
Outdoor Master recalled two models of children's and youth helmets on November 26, 2025. The helmets violate mandatory safety standards and pose a risk of serious head injury. Consumers should stop using them immediately and seek refunds.
Macardac recalled baby loungers on November 26, 2025, due to serious risks of entrapment and falls. The loungers violate safety standards for infant products. Consumers should stop using the loungers immediately and seek a refund.
Anzmtosn recalled its Magnet Fidget Spinner Sets on November 20, 2025, due to a serious ingestion hazard. The sets contain loose magnets that can pose a risk of severe injury or death to children. Consumers should stop using the product and seek a refund immediately.
Bearlala recalled baby loungers on November 20, 2025, due to risks of serious injury or death from entrapment and falls. The loungers do not meet mandatory safety standards for infant sleep products. Consumers should stop using the loungers immediately and seek a refund.
Zigjoy recalled children's sleep sacks on November 13, 2025, after discovering a violation of mandatory flammability standards. The recall affects sleep sacks sold in blue and pink, posing a serious burn risk to children. Consumers should stop using the sleep sacks immediately and contact Zigjoy for a refund.
Genepro Protein, Inc. recalled 250 bags of Genepro Whey 4th Generation Plasma Treated Protein on November 12, 2025. The product is mislabeled and fails to declare milk as an allergen, posing a serious risk to consumers with dairy allergies. The affected product has a 'Best By' date of February 13, 2027.
Olympus recalled 94 units of its 10 Fr. endoscopic sheath on November 11, 2025, due to complaints of the ceramic tip breaking. The defect poses a high risk for patients undergoing urological procedures. Healthcare providers and patients must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 55 SIBO Test units on November 3, 2025. The recall occurred due to distribution without premarket approval. Patients and healthcare providers should stop using this device immediately.
GET TESTED INTERNATIONAL AB recalled the GI Microbiome Profile XL on November 3, 2025, due to distribution without premarket approval. Three units were distributed nationwide in the U.S. Patients and healthcare providers should stop using this device immediately.
GET TESTED INTERNATIONAL AB recalled 940 Lyme tests on November 3, 2025. The recall occurred due to distribution without premarket approval. Healthcare providers and patients must stop using the product immediately.
Avenco and Novilla recalled mattresses on October 30, 2025, due to a fire hazard. The mattresses violate mandatory flammability standards, posing a risk of serious injury or death. Consumers should stop using the products immediately and contact the manufacturer for a remedy.
Bealife recalled 5,000 dressers on October 23, 2025, due to significant tip-over risks. The dressers can cause serious injuries or fatalities if not anchored to a wall. The recall involves model number AP23-W, which is only printed on the packaging.