immediate action Recalls

Meaicezli Play Purse Sets Recalled Over Battery Ingestion Risk

Currey & Company Recalls Electra Chandeliers Due to Fall Hazard

Pedego Electric Bikes Recalls Fat Tire Trikes Over Fall Hazards

This recall involves the Fat Tire Trike, an aluminum adult three-wheeled electric tricycle. It has a rectangular label on the downtube near the front of the frame with the word "Pedego" printed on it. The product was sold in matte black.

Imprimis NJOF Recalls Intraocular Injection Over Glass Particles

Presence of particulate matter - Glass like particles.

Blue Wave Recalls Above-Ground Pools Due to Drowning Hazard

TopHomer Pool Drain Covers Recalled Over Drowning Hazards

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.

Imprimis NJOF Recalls Intraocular Injection Due to Glass Particles

Presence of particulate matter - Glass like particles.

Imprimis NJOF Recalls Intraocular Injection Over Glass Particles Hazard

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.

Wilson-Cook Medical Recalls Bipolar Sphincterotomes Due to Hazard

Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting.

Rifton Equipment Recalls Low Base TRAM Due to Fraying Hazard

Potential for fraying on the body support strap.

Rifton Recalls E-Pacer Gait Training Device Over Fraying Risk

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.

Rifton Equipment Recalls TRAM Lift Device Over Strap Hazards

Potential for fraying on the body support strap.

CATAO MARKET Recalls Cuban Loaf Cake Over Undeclared Color Additive

CATAO MARKET recalled 3,120 Cuban loaf cakes on December 18, 2025. The recall follows the discovery of undeclared FD&C Yellow #5 in the product. This hazard poses a significant risk for consumers with allergies to this color additive.

CATAO MARKET Recalls Cuban Loaf Cake Over Undeclared Color Additive

Undeclared colors FD&C Yellow #5

CATAO MARKET Recalls Cuban Loaf Cake Due to Undeclared Color Additive

Undeclared colors FD&C Yellow #5

Rovira Biscuit Recalls Snack Crackers Over Undeclared Colors

Undeclared colors FD&C Yellow #6, and FD&C Red 40

Aju Pharm Recalls AlternatiV+ Max Knotless Anchor Due to Device Failures

Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.

H-E-B Coconut Yogurt Recalled for Undeclared Almonds

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.

Aju Pharm Co. Recalls Genesis Push-In Suture Anchor Due to Device Failures

Aju Pharm Co. recalled 200 units of the Genesis Push-In Suture Anchor on December 17, 2025. Users reported serious device failures including anchor breakage and suture breakage. Consumers and healthcare providers must stop using the device immediately.

Aju Pharm Recalls Screw-In Anchors Due to Device Failure

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.