Montana 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 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 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.

The recalled magnet games violate the mandatory standard for toys because they contain loose high-powered magnets that fit within CPSC's small parts cylinder, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

Mis-wired component-the improperly wired component can result in additional noise on the power supply output. Noise on the ultrasonic input circuit is not consistent with electromagnetic compatibility (EMC) standards and may decrease the overall reliability of the system and result in delay of treatment. It was discovered that additional serial numbers of ShockPulse generators may also have the mis-wired component. As a result, this is expanding the action to the additional impacted devices.

Behind-the-ear sound processer packaging label is different then included product.

Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life. Device expiry should have been calculated from gel impregnation (date of manufacture) but it was incorrectly calculated from device packaging.

The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values.