Consumer Product Recalls

Hazard: A short circuit increases the risk of a fire. In addition, the battery contactors may open suddenly and cause a loss of drive power, increasing the risk of a crash.

Hazard: A loose starter-generator connection can result in an engine stall, increasing the risk of a crash. In addition, the wiring may overheat, increasing the risk of a fire.

Hazard: An instrument panel display that fails to show critical safety information, such as the speedometer or warning lights, increases the risk of a crash.

Hazard: Liquid intrusion into a battery pack can cause a loss of electrical isolation or short circuit, increasing the risk of a fire or shock hazard.

Hazard: Incorrect belt orientation may cause the tires to fail and increase the risk of a crash.

Hazard: A sudden loss of drive power increases the risk of a crash.

Hazard: A rapid oil leak can result in an engine stall, increasing the risk of a crash. In addition, an oil leak in the presence of an ignition source such as hot engine or exhaust components, can increase the risk of a fire.

Hazard: An engine that overheats increases the risk of a fire.

Hazard: Loss of drive power increases the risk of a crash or injury.

Hazard: An unexpected increase in steering effort can result in a loss of control, increasing the risk of a crash.

Hazard: Incorrect head restraint information may lead to improperly adjusted head restraints, increasing the risk of injury in a crash.

Hazard: Windshield wiper failure can reduce driver visibility, increasing the risk of a crash.

Hazard: Reduced steering control, a brake fluid leak, and loss of front brake function increase the risk of a crash.

Hazard: The recalled children's bunk beds violate the federal regulations for bunk beds because the spacing between the guardrail and end support and the spacing around the mattress supports are greater than allowed, posing entrapment and strangulation hazards to children.

Hazard: The recalled dressers are unstable if they are not properly anchored to the wall, posing serious tip-over and entrapment hazards, and the two additional metal support legs also present tripping hazards. The dressers violate performance and warning label requirements of the STURDY Act.

Hazard: The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.

Hazard: The bike's protective chain/belt guard does not cover the belt drive and loose clothing can get entrapped in the belt drive, posing a fall hazard.

Hazard: The flame can burn too high and cause the candle to ignite and the glass container to break, posing fire, burn and laceration hazards.

Hazard: The recalled window shades have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window shades are in violation of the federal regulations for window coverings and present a substantial product hazard. The window shades also violate federal regulations for labeling of window coverings.

Hazard: The recalled jewelry-making kits contain a resin that, when liquid, can cause skin, eye and respiratory irritation or sensitization when inhaled, touched or ingested. The resin contains an acrylate (hydroxyethylmethacrylate "HEMA") in amounts prohibited in children's products by the Federal Hazardous Substances Act. Already created jewelry should be inspected to confirm it is fully cured. If there is liquid or any liquid residue present, the jewelry should not be worn and should be stored away from children. Once cured, the resin no longer presents the hazard.

Hazard: The incorrect computed patient age is showing in VX for patients less than 3 months old.

Hazard: During an internal investigation, ACS was unable to confirm that the CODMAN component achieved the required Sterility Assurance Level and therefore is not suitable for sterilization according to ACS procedures.

Hazard: Airway adapter does not meet specification and may break off when attaching a valve or tube. Device failure may result in inaccurate readings, a break in airway circuit, and loss of ventilation. A break in the airway circuit could result in inability to ventilate, hypoxia, cardiopulmonary collapse, or death.

Hazard: Airway adapter does not meet specification and may break off when attaching a valve or tube. Device failure may result in inaccurate readings, a break in airway circuit, and loss of ventilation. A break in the airway circuit could result in inability to ventilate, hypoxia, cardiopulmonary collapse, or death.

Hazard: Five complaints received where surgeon was unable to remove and/or connect the inserter with the stem during surgery due to excess material remaining within the taper. Issue may lead to clinically significant extension of surgery to find a replacement.

Hazard: When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

Hazard: When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

Hazard: When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

Hazard: When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

Hazard: When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.