Consumer Product Recalls

Hazard: The USB module in the recliner arm can overheat and spark, posing an overheating hazard.

Hazard: The recalled lithium-ion batteries can overheat, posing fire and burn hazards.

Hazard: The lithium-ion battery in the recalled power banks can overheat and ignite while charging, posing fire and burn hazards to consumers.

Hazard: The steamers can leak steam or spew hot boiling water, posing a risk of serious burn injury to users.

Hazard: The scented highlighters, which resemble cups with straws, contain phthalates; a violation of the federal phthalates ban. Phthalates are toxic if ingested by young children and can cause adverse health effects.

Hazard: The ramps cannot withstand the weight of equipment within the limits that are specified on the ramps and can bend or break while in use, posing a fall hazard.

Hazard: Due to the potential that some units within specific lots were damaged during the manufacturing process. The area of damage is within the same area of the lidding. While the damage in the lidding is visibly noticeable, due to risk of sterility being compromised.

Hazard: Due to the potential that some units within specific lots were damaged during the manufacturing process. The area of damage is within the same area of the lidding. While the damage in the lidding is visibly noticeable, due to risk of sterility being compromised.

Hazard: Due to the potential that some units within specific lots were damaged during the manufacturing process. The area of damage is within the same area of the lidding. While the damage in the lidding is visibly noticeable, due to risk of sterility being compromised.

Hazard: Due to manufacturing error, digital analog rotational feature is 180 degrees off.

Hazard: Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case scenario. Potential punctures may go undetected in clinical settings due to small size and variable location.

Hazard: Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case scenario. Potential punctures may go undetected in clinical settings due to small size and variable location.

Hazard: Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case scenario. Potential punctures may go undetected in clinical settings due to small size and variable location.

Hazard: Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case scenario. Potential punctures may go undetected in clinical settings due to small size and variable location.

Hazard: A mechanical component that supports the O2 gantry to the support structure in affected devices may have been damaged during manufacture.

Hazard: Product packaging contains the wrong part number and kit contents.

Hazard: Due to labeling error. Product incorrectly labeled.

Hazard: Unintended radial detector motion may occur during patient setup or during patient scan if system does not have correct version of gantry software installed. Unintended detector motion may result in life-threatening injury.

Hazard: Unintended radial detector motion may occur during patient setup or during patient scan if system does not have correct version of gantry software installed. Unintended detector motion may result in life-threatening injury.

Hazard: Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and will not prevent the user from using an expired material.

Hazard: Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and will not prevent the user from using an expired material.

Hazard: Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and will not prevent the user from using an expired material.

Hazard: Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and will not prevent the user from using an expired material.

Hazard: Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and will not prevent the user from using an expired material.

Hazard: due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.

Hazard: due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.

Hazard: due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.

Hazard: due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.

Hazard: due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.

Hazard: due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.