Consumer Product Recalls

Hazard: An upper triple clamp that fractures while the motorcycle is being operated could lead to a loss of control, increasing the risk of a crash.

Hazard: A damaged retractor may not properly restrain an occupant during a crash, increasing the risk of injury.

Hazard: Damaged wire may overheat and short, increasing the risk of a fire.

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

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

Hazard: Failure to detect another vehicle increases the risk of a crash.

Hazard: A door that cannot be opened may trap occupants inside the vehicle, increasing the risk of injury.

Hazard: The inability to use the horn or switch the headlight from low beam to high beam can increase the risk of a crash or injury.

Hazard: A loss of power steering assist can require greater steering effort, increasing the risk of a crash or injury.

Hazard: An engine shutdown increases the risk of a crash.

Hazard: Reduced structural integrity may increase the risk of injury in a crash.

Hazard: A damaged tire may blowout, increasing the risk of a crash.

Hazard: The trailer may be accidentally overloaded after referencing the incorrect information, increasing the risk of a crash.

Hazard: An inoperative defroster and defogger system can decrease the driver's visibility under certain driving conditions, increasing the risk of a crash.

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

Hazard: An incorrect cross beam may not adequately protect occupants in a crash, increasing the risk of injury.

Hazard: A vehicle rollaway increases the risk of a crash.

Hazard: An air bag with insufficient pressure retention increases the risk of ejection and injury during a crash.

Hazard: A door that cannot be opened may trap occupants inside the vehicle, increasing the risk of injury.

Hazard: A manufacturing defect allows the recalled chamber locks to be forcibly removed, allowing unauthorized or unintended access to the firearm, posing a risk of serious injury or death.

Hazard: The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard; and an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped. The portable loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.

Hazard: The flexible grease gun hose can develop a hole allowing grease to be ejected while using the grease gun, posing a laceration hazard.

Hazard: Kits contain SureStep Foley Tray Systems recalled by BD that include incorrect product information insert sheets. If a mislabeled tray is used, patient risk ranges from minor injury to injury that requires medical intervention, such as infection or local/systemic allergic reaction (anaphylaxis).

Hazard: Antivirus software was not consistently installed on impacted devices during the implementation process.

Hazard: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.

Hazard: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.

Hazard: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.

Hazard: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.

Hazard: During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further sterilization according to ACS procedures. As a result, ACS is unable to confirm product sterilization assurance requirements were met.

Hazard: During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further sterilization according to ACS procedures. As a result, ACS is unable to confirm product sterilization assurance requirements were met.