stop use immediately Recalls

FUJIFILM Healthcare Recalls X-ray Generator Over Fire Hazard

Maquet Cardiopulmonary Recalls Venous Bubble Sensor Due to Cable Risk

Maquet Cardiopulmonary Gmbh recalled 3,050 Venous Bubble Sensors on January 9, 2026. Internal investigations revealed issues with the durability of the connecting cable. Excessive bending can lead to device failure, posing a risk to patient safety.

Kalencom Recalls SARO Crib Bumpers Due to Suffocation Hazard

Kalencom Corporation recalled SARO Braided Crib Bumpers on January 8, 2026, due to suffocation risks. The bumpers can obstruct an infant's breathing, violating federal safety regulations. Consumers should stop using the product immediately and seek a refund.

Vasicar Dressers Recalled Due to Tip-Over Hazard

Vasicar recalled 18,000 dressers on January 8, 2026, due to tip-over risks. The dressers can cause serious injury or death if not anchored to the wall. Consumers should stop using them immediately and seek a refund.

Isla Rae Magnetic Wireless Chargers Recalled Over Fire Hazard

Marcus Adler Glove Recalls Pajama Pants and Shorts Over Burn Hazard

Marcus Adler Glove recalled Julie and Judah pajama pants and shorts on January 8, 2026. The products violate mandatory flammability standards for children's sleepwear. Consumers should immediately stop using these items and seek a refund.

Medline Recalls Dialysis Kits Over Risk of Seal Failure

Medline Dialysis Kits Recalled Over Silicone Seal Issues

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)

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.

Olympus Recalls Sphincterotome Due to Risk of Deformation

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