Nebraska recalls

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator

Lack of Assurance of Sterility

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Subpotent Drug: Low out of specification assay results performed during long-term stability testing.

July 21st, 2026, PT Organics Limited of Lake Oswego, Oregon is voluntarily recalling select Pumpkin Tree Peter Rabbit Organics Banana & Strawberry 4 oz. (113 g) pouches because of an internal packaging defect that may result in the presence of a strand of soft, food-grade plastic in the finished pro

Relay Peak Research LLC (Zen Principle Naturals) of Incline Village, NV is voluntarily recalling its Zen Principle® brand Moringa Capsules dietary supplement because the product has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections i

FOR IMMEDIATE RELEASE – July 18th, 2026 – Panoli, Gujarat, Unique Pharmaceutical Laboratories (A Div. of J. B. Chemicals & Pharmaceuticals Ltd.) is voluntarily recalling four lots of Cetirizine Hydrochloride Tablets USP 5 mg to the consumer level due to cross contamination with Ranitidine.

The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. Additionally, the bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.

The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard.

The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.

The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.

The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of serious injury or death from fire and burn hazards. In addition, the lighters failed to meet the pre-market lighter submission requirement needed to demonstrate that the lighters feature child-resistant mechanisms and ensuring their safety and compliance with U.S. regulations.

The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death.

The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning.

The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or children and can cause adverse health issues.

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.