Latest Product Recalls Today

Lamborghini (Automobili Lamborghini) is recalling certain 2024-2025 Revuelto vehicles. A software error may prevent the rearview camera image from displaying. 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.

Honda (American Honda Motor Co.) is recalling certain 2023 Honda Accord, Accord Hybrid, and 2024 HR-V, Pilot, and Acura Integra vehicles. The driver's seat cushion frame may not have been tightened properly, which can result in a loose seat. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 207, "Seating Systems." A loose driver's seat may not adequately restrain the driver during a crash, increasing the risk of injury.

Autocar, LLC (Autocar) is recalling certain 2023-2026 ACX (Xpeditor) vehicles. Contact with the drive line yoke may damage the Electronic Stability Control (ESC) unit. A damaged ESC unit may malfunction, disabling the electronic stability control and increasing the risk of a crash.

This recall involves Viofairy Hair Growth Serum. The hair serum comes in black and gold packaging and a black bottle with gold and white label and a black cap. The hair serum has "VIOFAIRY HAIR GROWTH SERUM" and "5% MINOXIDIL With BIOTIN" printed on labels located the front of the bottle.

This recall involves Sefudun 5% Minoxidil Hair Growth Serum Kit . The hair serum comes in a black glass bottle with a black and golden dropper cap and a black and white label. The kit included a black plastic applicator. The hair serum has "SEFUDUN HAIR GROWTH SERUM" and "BIOTIN 5% MINOXIDIL" printed on labels located on the front of the bottle.

This recall involves Mindbodygreen Ultimate Multivitamin+ dietary supplement bottles with the following UPC, lot numbers and manufacturing dates (Month/Year format). The dietary supplements come in eight-ounce amber glass bottles with black caps, each containing 60 capsules. The UPC, lot numbers and manufacturing dates are printed on the bottle. UPC Lot Number Manufacturing Date 850027975177 0515I1 09/2021 0130B2 01/2022 0187I2 08/2022 0324J2 10/2022 0309A3 12/2022 0368L2 12/2022 0272B3 02/2023 850027975429 0408H3 06/2023 0143A4 12/2023 0179C4 02/2024 4021131 05/2024 4033211 07/2024 4080841 10/2024 A010611 03/2025 A021211 03/2025

This recall involves LuxJet Submersible LED Lights. The LED lights were sold in sets of 10 LED color changing lights, two remote controls, 20 preinstalled CR2450 lithium batteries in the lights and four preinstalled CR2032 lithium batteries in the remote controls. Each light is about 3.5 cm in diameter.

This recall involves Bazic Silicone Glue, Model 2030. The glue comes in a transparent plastic bottle with a blue nozzle top and a blue and black wraparound label bearing instructions and warning statements. The glue's label reads "Bazic", "Silicone Glue", and "Clear Adhesive Sealant" on the front, with cautionary statements and "2030" above the barcode on its side. Only Bazic Silicone Glue with batch code "V01233-031725-70004523" printed on the side of the bottles are included in the recall.

This recall involves the AiTuiTui Pull String Teething Toy. The teething toy is an off-white disc shape with either a red ball or blue ball in the middle and six long pull string "tentacles" of various colors running through the ball. There are also three free-spinning rings on one side and soft push buttons on the disc. "Model: 688-59" is printed on the product packaging.

Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Potential for fraying on the body support strap.

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some ROI(s) which have no contours and either have a material override defined, or are of type Bolus, Fixation, or Support. In these cases, adding geometry to the ROI, subsequently modifying geometry, or removing the material override does not invalidate dose as intended.

Due to probe bags that may have a compromised or incomplete sterile pouch seal.

Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the performance claim listed in the Instructions for Use (IFU). LDL Cholesterol reagent showed clinically significant interference due to triglyceride concentration up to 1500 mg/dL may cause a maximum positive bias of up to 28.8% in low LDL Cholesterol samples (concentration 80 mg/dL) and up to 11.02% in high LDL Cholesterol samples (concentration 160mg/dL).

Software errors that can result in incorrect surgical instrument positioning during spinal surgery.

The supplier manufactured anatomical left plates with an incorrect thread orientation.

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Inflation device handle may detach from the syringe during procedure.

Under specific conditions, the lift's electromagnetic holding force may disengage unexpectedly, allowing unintended downward movement of the lift.