Pet food and pet product recalls

The vehicle can move when on an incline and "park" is displayed on the digital dash. This can allow the vehicle to roll away, posing a crash hazard.

The swing should never be used for sleep and bedding materials should never be added to it. If the product is used for sleep or bedding material is added, the headrest and body support insert on the seat pad can increase the risk of suffocation.

The recalled playpens violate the federal safety regulations for play yards. The included basketball hoop accessory can be a head entrapment hazard and children can become entrapped beneath the mattress, posing a suffocation hazard.

Products contains inorganic arsenic above action level set in guidance to industry.

Product contains elevated levels of lead (2,040ppb).

Product contains inorganic arsenic above action level set in industry guidance (13.2ppb)

The recalled baby loungers violate the federal safety regulations for Infant Sleep Products because the sides are too low to contain the infant; the sleeping pad is too thick, posing a suffocation hazard; an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped; and the loungers do not have a stand, posing a fall hazard if used on elevated surfaces. These violations create an unsafe sleeping environment for infants.

The pin on the u-joint of the steering knuckle was not swagged correctly, which can allow the pin to come out of the u-joint and cause the rider to lose steering control, posing a crash hazard.

The recalled area rugs violate the mandatory federal flammability regulations for carpets and rugs, posing a fire hazard.

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

The firm received reports that some blood collection tubes have experienced issues with clotting and poor separation due to missing additive. The failure of the device would likely require sample recollection which could result in a delay of treatment.

Undeclared Yellow No. 5

Potential Salmonella contamination

Possibly contaminated with Listeria monocytogenes

The frames of the recalled cargo bicycles can crack and can bend and break, posing a fall hazard to the rider.

The recalled conditioner can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed to Pseudomonas aeruginosa face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria.

The recalled engines can overheat, posing fire and burn hazards.

Trumpet Needle Guide ring can detach when excessive pressure is applied.

Trumpet Needle Guide ring can detach when excessive pressure is applied.

The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire

The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire

Salmonella typhimurium in organic basil

X-ray system C-arm may experience uncontrolled motion if 1) AC motor controller firmware has a faulty setting, 2) the Motor/gear assembly is worn, 3) CAT movement is driven at maximum speed and angulated more than 75 deg. from vertical, and 4) the emergency stop or touch guard is activated during the breaking sequence, which could lead to the C-arm hitting the patient or operator.

The steering caps, which are used to hold the handlebar in place, can crack and cause the handlebars to become unstable, posing a crash hazard.

When the recalled dog eyelid wipes are opened and in use, bacteria and fungi, which are organisms found widely in the environment, soil, and water, can be introduced and grow in the container, posing a risk of serious infection to people with weakened immune systems. Individuals with wounds may also be at higher risk of infection. People with healthy immune systems are not typically affected.

The recalled snowmobile's drive clutch can break, allowing fragments to escape the snowmobile shielding, posing a laceration hazard.

Due to complaints of particulates, residue, occlusions, and bent tips for sterile cannulas.

Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.