2,056 recalls tagged with “cpsc regulated”.
Imprimis NJOF, LLC recalled 778 boxes of Dexamethasone Moxifloxacin intraocular injection on December 18, 2025. The recall stems from the presence of glass-like particles in the product. Consumers and healthcare providers should stop using the product immediately.
Rifton Equipment recalled 470 E-Pacer gait training devices on December 18, 2025. The body support strap may fray, posing a risk to users. Health care providers and patients must stop using the device immediately.
Imprimis NJOF, LLC recalled 314 boxes of Tri-Moxi+¿ intraocular injections on December 18, 2025. The recall is due to the presence of glass-like particles in the product. Consumers and healthcare providers should stop using the product immediately and contact the company for further guidance.
Imprimis NJOF, LLC recalled 596 boxes of intraocular injections on December 18, 2025. The recall affects products due to the presence of glass-like particles. Consumers should stop using the product immediately and contact their healthcare provider.
CATAO MARKET recalled 775 cases of Authentic Cuban Loaf Cake on December 18, 2025. The recall stems from an undeclared color additive, FD&C Yellow #5, which poses a significant health risk. Consumers should not eat the product and should seek a refund or replacement.
Rifton Equipment recalled 3,238 TRAM powered lift devices on December 18, 2025, due to a risk of fraying body support straps. This recall affects models K310 sold worldwide, including the US, Europe, and Australia. Healthcare providers and patients must stop using the devices immediately to prevent injury.
Blue Wave recalled all above-ground pools 48 inches and taller on December 18, 2025, due to a drowning risk. The pools may allow children to access the water even when ladders are removed. Consumers should stop using these pools immediately and contact Blue Wave for a free repair kit.
TopHomer recalled pool drain covers on December 18, 2025, due to serious entrapment and drowning hazards. The recall affects 8-inch drain covers sold on Amazon. Consumers should immediately stop using the products and seek refunds.
17 Stories Furniture recalled 18-Drawer Dressers on December 18, 2025, due to tip-over and entrapment hazards. The dressers pose a serious risk of injury or death to children if not anchored to the wall. This recall affects models HI1382_13, HI1382_01, and HI1382_09.
Vascutek recalled 37,430 Gelsoft Plus and Gelweave vascular prostheses distributed nationwide in the United States after discovering the devices were labeled with an extra month of shelf life. The expiry date was calculated from packaging rather than gel impregnation. Healthcare providers and patients should stop using the devices immediately and follow recall instructions.
Aju Pharm Co. recalled 600 units of Genesis Screw-In Anchors on December 17, 2025. Reports indicate serious device failures, including anchor breakage and suture breakage. Healthcare providers and patients should stop using these anchors immediately.
Prima Foods International recalled 12,214 bottles of BarbaCuban 455 Everything Sauce on December 17, 2025. The sauce contains undeclared quinine, posing a health risk to consumers. Affected products were distributed in Florida with best by dates from January to June 2026.
Aju Pharm Co. recalled 400 Dual Thread Screw-In Anchors on December 17, 2025. The recall follows reports of device failures including breakage and pull-out incidents. Healthcare providers and patients should stop using these devices immediately.
Aju Pharm Co. recalled 416 units of its AlternatiV+ Screw-In Anchor on December 17, 2025, after reports of significant device failures. The defects include anchor breakage, bending, and suture breakage. Patients and healthcare providers should stop using the device immediately.
Prima Foods International recalled 12,214 bottles of BarbaCuban Havana Gold due to undeclared quinine. The recall affects products distributed in Florida. Consumers should not consume the product and seek refunds immediately.
Aju Pharm Co. recalled 233 Fixone Hybrid Anchors on December 17, 2025, due to multiple reports of device failures. The issues include anchor breakage, bending, and suture breakage. Patients and healthcare providers must stop using the device immediately.
Rovira Biscuit Corporation recalled 29,246 units of Tita Crackers on December 17, 2025. The recall stems from undeclared colors FD&C Yellow #6 and FD&C Red 40. Consumers in GA, TX, MA, IL, MD, USVI, and Puerto Rico should not consume these products.
H-E-B recalled 175 cases of Higher Harvest Dairy Free Coconut Based Yogurt on December 17, 2025. The product contains undeclared almonds, posing a serious allergy risk. Consumers should stop using the yogurt immediately and contact the company for refunds.
Prima Foods International recalled 12,214 bottles of its 90 Miles to Mojo Marinade on December 17, 2025. The product contains undeclared quinine, posing a serious health risk. Consumers should not consume this product and should seek a refund immediately.
Rovira Biscuit Corporation recalled over 22,000 boxes of Vanilla Econo cookies on December 17, 2025. The recall affects cookies containing undeclared colors FD&C Yellow #6 and FD&C Red 40, which may pose health risks. The affected products were distributed in Georgia, Texas, Massachusetts, Illinois, Maryland, the U.S. Virgin Islands, and Puerto Rico.