cpsc regulated Recalls

Imprimis NJOF Recalls Intraocular Injection Due to Glass Particles

Presence of particulate matter - Glass like particles.

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.

JOKOSIS Bed Rails Recalled for Entrapment and Asphyxiation Risk

This recall involves JOKOSIS Bed Rail, model HC0262. The bed rails are black and include a zippered storage pouch. The product measures 31.5 inches tall by 40.6 inches wide. The bed rail has model "HC0262" printed on the packaging.

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

Rifton Equipment Recalls TRAM Lift Device Over Strap Hazards

Potential for fraying on the body support strap.

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.

CATAO MARKET Recalls Cuban Loaf Cake Due to Undeclared Color Additive

Undeclared colors FD&C Yellow #5

KKL Fabric Dressers Recalled Over Tip-Over Hazard

17 Stories Furniture 18-Drawer Dressers Recalled Over Tip-Over 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.

Prima Foods Recalls Ketchup Over Undeclared Quinine Hazard

Rovira Biscuit Recalls Vanilla Econo Cookies Over Undeclared Colors

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

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.

Aju Pharm Recalls Dual Thread Screw-In Anchors Over Device Failures

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.

BarbaCuban White Truffle Sauce Recalled for Undeclared Quinine

BarbaCuban recalled 12,214 bottles of White Truffle Sauce on December 17, 2025, due to undeclared quinine. The affected product poses a high risk to consumers. Customers should not consume the sauce and seek refunds immediately.

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 Recalls Screw-In Anchor Due to Device Failure Risks

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

Aju Pharm Recalls Fixone Hybrid Anchor Due to Device Failures

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.

Prima Foods Recalls BarbaCuban Havana Gold Over Quinine Hazard

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.