Latest Product Recalls Today

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 all Sunneday and Blue Bay brand above-ground pools 48 inches and taller. Model information and the Sunneday or Blue Bay logo are printed on the liner on the outside of the pool. Pool models subject to this recall include: Model Description UPC Code 70018 Sunneday Oasis Cottage 18'x52" 850022858529 70024 Sunneday Oasis Cottage 24'x52" 850022858536 358015W Blue Bay Softsided Pool 15'x48" 191127003583 359015G Blue Bay Softsided Pool 15'x48" 191127003590 360018W Blue Bay Softsided Pool 18'x52" 191127003606 361018G Blue Bay Softsided Pool 18'x52" 191127003613 380018T Blue Bay Softsided Pool 18'x52" 191127003804 The recalled above-ground pools contain a compression strap (also referred to as a reinforcing belt) that wraps around the pool on the outside of the vertical support poles, and may create a foothold, allowing a child to access the pool and drown. Children can still gain access to the pools using these footholds even if the ladder is removed. CPSC's website www.PoolSafely.gov has free, downloadable educational materials available to the public on pool safety including information on barriers, covers, alarms and other safety information.

This recall involves a Giraffe Plush Toy with clip and a Llama Plush Toy with clip. The Giraffe with clip has a yellow body with a yellow claw clip. The legs of the giraffe are orange and blue with various colored paws. The ears are black and white animal print. The Giraffe measures about nine inches long. The Giraffe has "HL699436 or HL731481" printed on the white sewn-in label. The hang tag on the Giraffe has "2553675" printed on the front left corner. The Llama with clip has a white body with a green claw clip. The body has a mirror and orange triangle teether attached to the body. The legs of the Llama are orange and yellow with various colored paws. The Llama measures about 12 inches long. "HL699436" is printed on the white sewn-in label attached to the body. The hang tag on the plush has "2553634" printed on the front left corner.

This recall involves Urban Arrow FamilyNext Pro Cargo E-Bikes with Fidlock buckles. The recalled bicycle comes in one size and comes in green and black. The frame of the bicycle is made of aluminum with a reinforced foam (EPP) cargo box. The bicycle is 105" in length and 28" wide. "Urban Arrow" is imprinted on the bottom of the cargo box.

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.

Due to products not having FDA Premarket authorization to be distributed within the United States.

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.