Consumer Product Recalls

Hazard: The door panel may remain in the open position or open unexpectedly, increasing the risk of passenger being injured falling out of the bus.

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

Hazard: A fuel leak in the presence of an ignition source increases the risk of a fire.

Hazard: An instrument panel display that does not show critical information can increase the risk of a crash or injury.

Hazard: An indicator light that does not illuminate may fail to warn the driver of an ESC system issue, increasing the risk of a crash.

Hazard: Detached trim pieces can create a road hazard for other vehicles, increasing the risk of a crash.

Hazard: An inflator rupture may result in sharp metal fragments striking occupants, resulting in injury.

Hazard: Turn signals and tail lights that fail to illuminate or flicker can reduce visibility, increasing the risk of a crash.

Hazard: A loose or detached seat assembly increases the risk of injury.

Hazard: The recalled children's pajama sets violate mandatory standards for children's sleepwear flammability, posing a risk of burn injuries to children.

Hazard: The recalled toy is intended for children under three years of age and contains small parts, which violates the small parts ban, posing a deadly choking hazard.

Hazard: The recalled multivitamins contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The recalled packaging of the iron-containing multivitamins violates the federal standard for child-resistant packaging because the bottle caps are not child-resistant, posing a risk of deadly poisoning, if the contents are swallowed by young children.

Hazard: The recalled mini fridge's electrical switch can short circuit, causing it to overheat, posing a fire and burn hazard.

Hazard: Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.

Hazard: Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.

Hazard: Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.

Hazard: Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.

Hazard: Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.

Hazard: Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.

Hazard: Due to an incorrect test results provided that indicated the incorrect drug therapy recommendation

Hazard: Surgical drape packs may have open seals, which may compromise the sterility of the product.

Hazard: The potential of the elastic bands included in the kit detaching or fracturing during surgical procedures. As a result, these failures may pose a risk of retained foreign bodies in the surgical cavity and potentially leading to surgical site infections.

Hazard: Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an issue with the Schiller ARGUS PB-3000 Patient Data Module (PDM) where certain units trigger an error message on the Merge Hemo Client (Pressure Sensor Defective) during non-invasive blood pressure (NIBP) measurements, specifically when the initial inflation pressure is set in the high-pressure range (>240 mmHg). The ARGUS PB-3000 is a vital signs monitoring instrument intended to be integrated into the Merge Hemo System. No other components of the Merge Hemo System are affected.

Hazard: Flowmeter patch as a human readable expiry date on the outer shipping packaging that reads 2025-06-20 when it should read 2026-06-20.

Hazard: Potential for missing pins at tip of inserter.

Hazard: Due to a risk of false positive results that could lead to unnecessary medical treatment.

Hazard: Engaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the connection geometry; if the flat is on the wrong side of the post, the crown will not fit onto the abutment in the correct orientation, resulting in restoration delay.

Hazard: Bone external fixation system may have the pin that can become dislodged resulting in frame instability, the use of this product may cause a delay in surgery or a revision if the device is use.

Hazard: Packaging failures were identified which could lead to a breach in the sterile barrier.

Hazard: Packaging failures were identified which could lead to a breach in the sterile barrier.