All Product Recalls

Rattan 6-Drawer Dressers Recalled Over Tip-Over Hazard

Island Crab Recalls Smoked Grouper Dip Over Allergen Risks

Island Crab Corporation recalled 23 units of Smoked Grouper Dip on January 8, 2026. The product contains undeclared allergens including milk, eggs, and sodium metabisulfite. Consumers should not consume this product and seek a refund.

Medline Recalls Dialysis Kits Over Risk of Seal Failure

Medline Dialysis Kits Recalled Over Silicone Seal Issues

Outside The Breadbox Bread Crumbs Recalled Due to Allergens

Outside The Breadbox recalled 4,497 units of bread crumbs on January 8, 2026. The product contains undeclared allergens: egg and milk. Consumers in CO, MS, ND, NE, RI, TN, TX, and WI should not consume the product.

Medline Recalls Tego Connectors Over High Risk of Fluid Leakage

Medline Medical Kits Recalled Due to High Hazard Risk

Medline Dialysis Kits Recalled Over Risk of Fluid Leakage

Medline Industries recalled 2,020 dialysis kits on January 8, 2026, due to defective silicone seals. The seals may dome or tear, leading to fluid leaks and contamination. Patients and healthcare providers should stop using these kits immediately.

Medline Recalls Dialysis Dressing Change Kits Over High Hazard

Olympus ShockPulse-SE Lithotripsy System Recall Expands to 55 Units in 5 Countries (2026)

Medline Recalls Convenience Kits Over Sterility Concerns

Medline Industries recalled 9,720 convenience kits on January 7, 2026, due to sterilization calibration issues. The affected products may not meet sterility assurance levels. Patients and healthcare providers should stop using these kits immediately.

Medline Recalls Convenience Kits Over Sterility Issues

Olympus Medical Device Recalled Over Deformation Risk

Devices which did not undergo thermoforming could deform and lose performance.

Olympus Recalls Sphincterotome Over Deformation Risk

Devices which did not undergo thermoforming could deform and lose performance.

Olympus Recalls Sphincterotome Over Performance Risks

Devices which did not undergo thermoforming could deform and lose performance.

Olympus Sphincterotome Recalled Due to Deformation Risk

Olympus Corporation recalled 1,474 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to improper thermoforming. Healthcare providers and patients must stop using these instruments immediately.

Olympus Recalls Sphincterotome Over Performance Risks

Devices which did not undergo thermoforming could deform and lose performance.

Olympus Recalls Sphincterotome Due to Performance Risk

Devices which did not undergo thermoforming could deform and lose performance.

Olympus Recalls Sphincterotome V Due to Deformation Risk

Devices which did not undergo thermoforming could deform and lose performance.

Olympus Sphincterotome Recalled Due to Performance Risks

Devices which did not undergo thermoforming could deform and lose performance.