Latest Product Recalls Today

Forest River bus, LLC (Forest River Bus) is recalling certain 2025-2026 Trans Tech school buses. The modified seating floor plan may exceed the the rear Gross Axle Weight Rating (GAWR). As such these vehicles fail to comply with the Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - Other Than Passenger Cars." Overloading the rear axle may cause loss of vehicle control, increasing the risk of a crash.

Lucid USA, Inc. (Lucid) is recalling certain 2022-2026 Air vehicles equipped with an AD02 package and operating a software version from 2.8.0 through 2.8.16. The rearview camera image may not display when the vehicle is placed in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility." A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.

Hyundai Motor America (Hyundai) is recalling certain Genesis 2025-2026 G80, GV80, 2026 G80 "Electrified," GV60, GV70 "Electrified" and GV70 vehicles. Due to a software error, the instrument panel display may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays." An instrument panel display that fails to show critical safety information, such as the speedometer or fuel gauge, increases the risk of a crash.

Lucid USA, Inc. (Lucid) is recalling certain 2025-2026 Gravity vehicles operating a software version prior to 3.3.20. The rearview camera image may not display when the vehicle is placed in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility." A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.

This recall involves KEAWIS crib mattresses. KEAWIS crib mattresses were sold in white and measure about 38 inches by 24 inches. Model number "XX-BM-01" is printed on a label sewn on the side of the mattress.

This recall involves Ruahouine Hair Growth Serum. The serum comes in 60ml (2.11 fl. oz.) transparent amber dropper bottles. "Ruahouine", "Minoxidil Hair Growth Serum", and "5% Minoxidil With Biotin" are printed on labels wrapped around the bottles.

This recall involves RootStim Beard Growth Serums spray bottles. The serums come in black boxes with orange and white lettering and have an orange mustache icon on its front panel. The boxes have "Beard Growth Treatment" and "5% Minoxidil - Biotin & Rice Water" printed on its front, directions and warnings printed on its sides, and "Distributed By RootStim LLC" on the bottom. The bottles are black with black spray cap, transparent top cap, and an orange and black wraparound label bearing the same information as the box.

This recall involves R.X.Y-branded adult bike helmets. The recalled helmets were sold in one size fitting a head circumference of about 22.44 to 24.41 inches. The helmets are blue with black and have gray padding, black straps with a silver reflective pattern in the center and a black and red buckle with a gray chin strap. The helmets have a black plastic knob at the back of the helmet for adjusting the fitting. Item number "Kx012" is printed on the helmet's instruction manual.

This recall involves Morgan Lane Asher Pajama Sets, Style 816TR in Petal. The recalled children's pajama sets are printed with tiny roses and have blue cotton piping and imitation mother-of-pearl buttons. The pajamas were sold in sizes 2T to 14. "MORGAN LANE" and "PURE COTTON" are printed on labels located in the neck and waistband, and "100% Cotton Made in India" is printed on the side seam label.

This recall involves HEZI brand power strips. The HEZI power strip has either a gray or yellow metal enclosure with eight receptacles made of black plastic. There are a power and a circuit breaker switch located at the end of the metal enclosure closest to the power cord.

This recall involves Greatale self-feeding pillows. The recalled self-feeding pillows are made of stuffed fabric and have an elastic sleeve to hold a bottle in front of an infant's face. They were sold in white with angel wing shaped decorations. "Greatale" is on a label sewn into the seam of the pillow.

This recall involves BBWOO baby loungers. The recalled baby loungers are made of a foam sleeping pad and padded bumpers with a cloth cover and have a ribbon tie at one end. The model number is located on a tracking label stitched on the outside cover. The baby loungers were sold in the following styles and models: Style Model Number Gray Dinosaur BLG26BE Blue Car BLG23BD Green Line BLG04BD Gray Feather BLG01BE Pink Deer BLG17BI Pink Elephant BLG32BI Gray Line BLG04BE Blue CZC44 Gray CZC41 Khaki-Cotton & Velvet CZC43 Red CZC42

Rivian Automotive, LLC (Rivian) is recalling certain 2022-2025 R1T and 2022-2026 R1S vehicles. The bolts that secure the second-row driver and passenger side seat belt retractor assemblies may be improperly tightened. An improperly secured seat belt retractor may not adequately restrain the seat occupant, increasing the risk of injury during a crash.

Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.

Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.

Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.

It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength changed quickly.

Device packaged in incorrect outer box carton.

Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as delay of treatment or incorrect treatment.

Devices are not suitable for organ transplant.

A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When switching quickly between organ programs (OGPs) the collimation may be incorrect.

Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If healthcare providers base clinical judgment on unvalidated measurements, this could potentially lead to incorrect clinical decisions.

The affected lots show a decline in performance over time, which may lead to false-negative results.

Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays, requirement for alternate head fixation methods, and risk of patient injury.

Devices are not suitable for organ transplant.