Latest Product Recalls Today

Chrysler (FCA US, LLC) is recalling certain MOPAR tail lights with part numbers 68272126AC, and 68272127AC. The terminals in the tail light wiring harness may be damaged and cause the tail lights to fail. As such, this equipment fails to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment." Tail lights that fail to illuminate properly reduce the vehicle's visibility to other drivers, increasing the risk of a crash.

This recall involves VQQQ-branded natural gas patio heaters, models VQQQ-A1 and VQQQ-001. They have a bronze pole with a round base and a silver mushroom-shaped top with an adjustable height of 55 inches to 78 inches. A 24-foot-long gray gas hose is attached to the heater's base. The brand and model numbers are printed on the product's purchase receipt.

This recall involves CIYTI Light-Up Princess Costumes. The costumes include a blue dress with a crown and wand that light up, and a remote control. The crowns, scepters, and remote controls contain button batteries. There are no markings on the product. The package has "CIYTI" on the front.

This recall involves Costway high chairs designed to convert into a table and chair set. They were available in several color combinations, including purple and white, red and white, blue and white, and brown and white. There is no tracking information located on the products.

This recall involves Bamamon LED Projecting Finger Light toys which contain three button cells batteries. The finger lights come in 32 pieces in a box in red, orange, blue, black, purple, clear, green and yellow. The finger lights project eight space themed patterns such as astronauts, rockets, UFO, galaxy and solar systems printed on labels located on the front of the package.

PACCAR Incorporated (PACCAR) is recalling certain 2022-2023 Kenworth T370, T270, 2022-2027 Kenworth T280, Peterbilt 548, 2023-2027 Kenworth T480, T380, Peterbilt 536, 537, and 2025 Peterbilt 567 vehicles. The remote fuel filter hoses may separate from the fitting, causing a fuel leak and an engine stall. A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.

Undeclared Lobster

Undeclared colors (FD&C Blue No. 1 and FD&C Yellow No. 5)

Foreign object: May contain pieces of metal

defective packaging; packaging can rupture/explode during cooking.

May contain undeclared aspartame.

Undeclared soy.

Foreign object: May contain pieces of metal

If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemistry may escape from the bottle when the cap is twisted during opening, which could result in user exposure if required personal protective equipment (PPE) is not properly used. Such exposure may result in injury to the user or others in close proximity.

Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly.

Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this device configuration.

Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results

Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization.

Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.

Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device.

Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.

Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.

Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated.