Latest Product Recalls Today

This recall involves the Energizer® Large Power Indicator Lantern. The lantern is a cone-shaped portable light with an opaque lens and "Energizer" displayed on the side. The top portion of the lantern is gray with a large power button on top and a red handle. The model number of the lantern is BGAAL9 and the SKU number is 039800143341 or 039800143334. The model is located on the bottom of the light, on the removable cover that provides access to the charging cord storage area. The SKU is located on the packaging. Only lanterns with a date code of June 2024 located on the base of the unit, are part of this recall. The date code is shown using two circles, one circle has an arrow pointing to the year ("24"), and the other has an arrow pointing to the month ("6").

This recall expansion involves Curtis International 6-can minifridge model EFMIS121. This is in addition to certain minifridges with model numbers EFMIS129, EFMIS137, EFMIS149 and EFMIS175 that were previously recalled. "Frigidaire" is printed on the front of the units. The model and serial numbers are on a label on the back of the minifridge. This recall includes only the serial numbers identified below. The minifridges were sold in red at Target stores. Model Number Serial Number EFMIS121 Between A2001 and A2310

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

This recall involves Adirondack-style patio chairs sold under two different brands: Adams RealComfort and StyleWell. The resin chairs with slat backs and seats were sold in blue, dark gray, navy blue, taupe, light blue, lime green and teal. "ML837-15" and the manufacture date of August 2025 are molded on the underside of the recalled chairs. The manufacture date is indicated by a dot on a grid, located at the intersection of column "A" and row "25".

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.

Gulf Stream Coach, Inc. (Gulf Stream) is recalling certain 2026 Trail Boss and Ameri-Lite trailers. Wires in the taillight harness may be reversed, causing the turn signals to activate in the opposite direction as the driver intended. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment." Turn signals that fail to indicate the driver's intention to change direction increase the risk of a crash.

Ford Motor Company (Ford) is recalling certain 2013-2018 Focus, 2013-2019 Escape, and 2015-2016 MKC vehicles equipped with a 2.0L engine. The engine block heater may crack and develop a coolant leak, causing it to short circuit when the block heater is plugged in. An electrical short circuit can increase the risk of a fire.

Ford Motor Company (Ford) is recalling certain engine block heaters, with part numbers CV6Z-6A051-CA and CV6Z-6A051-AA, sold as accessory parts for certain 2013-2019 Ford and Lincoln vehicles equipped with 2.0L engines. The engine block heater may crack and develop a coolant leak, causing it to short circuit when the block heater is plugged in. An electrical short circuit can increase the risk of a fire.

Ford Motor Company (Ford) is recalling certain 2016-2018 Focus, 2019 Explorer, and 2024 Explorer vehicles. The engine block heater may crack and develop a coolant leak, causing it to short circuit when the block heater is plugged in. An electrical short circuit can increase the risk of a fire.

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.

Devices are not suitable for organ transplant.

Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple attempts. If this issue occurs, the instrument will be unable to complete initialization and transition to Ready mode and the instrument will not process patient samples, QCs or calibrators. This causes delayed results.

Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple attempts. If this issue occurs, the instrument will be unable to complete initialization and transition to Ready mode and the instrument will not process patient samples, QCs or calibrators. This causes delayed results.

Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient may experience shortness of breath leading to hypoxia, which may require medical intervention to prevent further respiratory deterioration.