Nebraska recalls

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place.

It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS does not interrupt the beam delivery if the Healthy Signal from an external gating device is lost. This may lead to a risk of mistreatment when external gating devices are used.

During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.

Product contains undeclared Yellow #5

Product contains undeclared Yellow #5

Product may be contaminated with Salmonella

Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.

The rivets used to support the swing seat can fail, posing a fall hazard to children.

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.

The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability, labeling and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.