Delaware recalls

The LED lights on the recalled illuminated spheres can overheat, posing a risk of serious injury or death from a fire hazard.

The recalled glasses violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries can be accessed easily by children, posing an ingestion hazard.?Additionally, the packaging and product do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

The recalled portable hook-on chairs violate the mandatory standard for portable hook-on chairs because the crotch restraints can be removed without the use of a tool and infants can fall through an opening, posing a deadly fall hazard.

The recalled Orb Funkee squeeze toys may contain fibrous tremolite (asbestos) in the sand, which can cause adverse health issues if inhaled.

The recalled resistance bands can forcefully separate from the handle during use, posing a risk of serious injury from impact hazard.

The recalled children's toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed by children, posing a deadly ingestion hazard to children. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

Chicago (May 20, 2026) – Hometown Food Company, in cooperation with Element Food Solutions, today initiated a limited, voluntary recall of a single lot code of its Birch Benders 12oz Sweet Potato Pancake Mix because it may contain undeclared egg. People who have an allergy or severe sensitivity to e

Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest. However, in rare cases, the steps may be displayed out of order. If this occurs, the programmed Flex Infusion schedule will not be delivered at the intended time, if at all.

Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to increased vessel wall stress, neointimal hyperplasia, vessel injury/rupture; if undersized may lead to incomplete expansion/malposition, acute stent thrombosis, distal embolization, ischemic neurological events

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product

Incomplete seals on sterile product