Latest Product Recalls Today

This recall involves Hydromassage rotary jets (6 fin) in Highlife Collection spas and also sold as replacement parts. There are eight models included in this collection: Grandee, Envoy, Vanguard, Aria, Prodigy, Sovereign, Jetsetter and Jetsetter LX. The recalled jets are found in model year 2023, 2024 and 2025 Highlife Collection spas.

This recall involves Colombia-themed magnetic board games. The recalled games consist of a two-sided board with a storage bag and 32 multi-colored magnetic pieces and two dice with one storage pouch. The original packaging included a piece of chocolate. "Colombia que linda eres" is printed on the game's board. "Cositas Colombianas" is printed on the front of storage box. Only the four- and six-player versions of the board games are included in this recall.

This recall involves Fortemotus-branded adult portable bed rails, model USFTMTJAS008. The recalled bed rails have black tubing with black foam rubber handle grips, support legs and a fabric pouch, and measure about 30 inches wide by 30 inches high. The Foremotus logo is printed on the bed rail's fabric cover and the model number on the owner's manual.

This recall involves CheerKid-branded baby bath seats. The recalled bath seats are sold in gray, pink and light blue. They come with five suction cups on the bottom and have a multi-colored rolling abacus toy at the front. "Model: BH-222" is printed on a label on the back of the bath seat.

This recall involves Beloems-branded adult portable bed rails, model BL-BR201. The recalled foldable bed rails have white metal tubing with either rounded black or gray foam rubber handle grips, support legs and a fabric pouch. The "Beloems" logo is printed on the bed rail's fabric cover and the model number on the owner's manual.

Nissan North America, Inc. (Nissan) is recalling certain 2023-2025 Rogue vehicles equipped with 3-cylinder 1.5L variable compression turbo (VC-Turbo) engines. Increased temperatures can break down the engine oil, which may cause the engine bearings to seize and become damaged, leading to engine failure. Engine failure can cause a loss of drive power, increasing the risk of a crash. A bearing failure may cause a breach in the engine block, allowing hot oil to be discharged, increasing the risk of an engine fire.

Nissan North America, Inc. (Nissan) is recalling certain 2024-2025 Rogue vehicles equipped with 3-cylinder 1.5L variable compression turbo (VC-Turbo) engines. The gears in the electronic throttle body assembly may break. Broken throttle body gears can cause a loss of drive power, increasing the risk of a crash.

General Motors, LLC (GM) is recalling certain 2024 Lyriq vehicles. The rearview camera screen may turn gray with no camera image. An inoperative rearview camera can reduce the driver's rear visibility, increasing the risk of a crash.

General Motors, LLC is recalling certain 2020 Chevrolet Silverado 2500, 3500, GMC Sierra 2500, 3500, and 2020-2022 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles that may have been repaired incorrectly under recall 24V797. The transmission control valve may fail and cause the rear wheels to lock up. Rear wheel lock up increases the risk of a crash.

International Motors, LLC (International) is recalling certain 2026-2027 MV vehicles. The ECU software may fail to engage the brakes with adaptive cruise control (ACC) or hill hold assist. A vehicle that does not automatically brake as expected increases the risk of a crash.

This recall involves Ammo Tabs, rectangular, off-white fiber desiccant tiles measuring about 2 inches by 4 inches with a thickness of 2.5mm. The tiles are used within ammunition cans and pistol cases to absorb and lock in humidity. Model number AMT-010 is printed on the packaging.

This recall involves Aroeve brand air purifiers, model MK04. The recalled air purifiers come in black or white. The model, date code, and serial number information are printed on the product label located on the bottom of the air purifiers. The air purifiers subject to this recall were manufactured prior to July 2025 and have a serial number starting with "BN".

This recall involves SOOWERY 6-Drawer Dressers. The dressers were sold in black. They have a metal frame, wooden top, and six collapsable fabric drawers. The dressers are 47.2 inches long by 11.8 inches wide by 33.3 inches tall.

This recall involves 3-Pack Smoke Detector Fire Alarms. The alarms are 9V battery operated and have a light sound warning and test button. The alarms are white and circular in shape. Model number "XG-7D04-KZ9Z" and SKU number "CX-50YP-A5VN" are printed on the bottom side of the alarm.

Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.

Due to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use. This test was supposed to be used to detect Universal Surgical Manipulator insertion axis ball screws that exhibit the symptoms of being bent and misaligned which is a precursor to potential ball screw fatigue failure/fraction

Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).

A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.

Devices which did not undergo thermoforming could deform and lose performance.

Nasal feeding tube packaged without the nasal transfer tube component.

942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discrepancy, which may cause surgical delay to exchange devices or revision surgery.

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.