Latest Product Recalls Today

Prevost Car (US) Inc. (Prevost) is recalling certain exterior driver side mirrors with part number 990648. The mirror exhibits excessive play and may detach. A detached mirror can reduce the driver's visibility and become a road hazard for other vehicles, increasing the risk of a crash.

Prevost Car (US) Inc. (Prevost) is recalling certain 2026 H3-45 and H3-45 VIP vehicles equipped with aftermarket exterior driver side mirrors. The mirror exhibits excessive play and may detach. A detached mirror can reduce the driver's visibility and become a road hazard for other vehicles, increasing the risk of a crash.

Jaguar Land Rover North America, LLC (Land Rover) is recalling certain 2023-2026 Range Rover Sport and Range Rover vehicles. The panoramic sunroof side finisher trim may not be properly secured and can detach. A detached panoramic sunroof side trim can become a road hazard, increasing the risk of injury or crash.

This recall involves Vive Health Bed Rails, model LVA1024 and LVA3031BLK. The model LVA1024 bed rail comes in a white frame with a black handle and measures 20 inches wide by 32 inches tall. The model LVA3031BLK bed rail comes in a black frame with a black handle and measures 13 inches wide by 18 inches tall.

This recall involves SAMIT multi-purpose helmets for children. The recalled helmets were sold in one size and fit a head circumference of about 21 to 23 inches. The helmets are sold in "crack" blue, "crack" red, and "crack" black with a cracked paint design. They were also sold in pure black. The helmets have gray padding, black straps, a black and red buckle with a black chin strap, and a black plastic knob at the back of the helmet for adjusting the fitting.

This recall involves Prismatic 3D Prints Book Nooks with Lights. The book nooks are bookshelf decorations meant to be placed in between books. The book nooks come in three designs: Fantasy Window, Gothic Cathedral Window, and Gothic Cathedral Window that are a set of three. The book nooks were sold in a variety of different colors for the frame and window. Frame colors include antique gold, pewter, black granite, white marble, and black. Window colors include purple, red, yellow, green, and blue. The base of the book nooks has a circular recess behind the window for holding spare CR2032 coin cell batteries. The words "extra battery" is embedded in the plastic in the recess.

This recall involves Joly's 80% Vinegar (32-ounce, pack of two). The vinegar comes in a white capped transparent bottle with an orange and red label with white lettering that has "Joly's" brand, "80% Vinegar" and "Dilutes to 5 Gallons". There are no other markings on the container.

This recall involves JJGoo- branded balloon lights. The recalled, submersible lights were sold in packs of 100 LED color-changing lights. Each multi-color, blinking light measures about 0.6 inches in diameter and has 200 preinstalled LR41 batteries. "MY1005E-Colorfu1-100" is printed on a label on the product packaging.

This recall involves Huaker Magnetic Balls and Rods sets. The sets include 88 pieces and come in a plastic box with a handle. "Magnetic Sticks" and "Model:20A-13" are printed on the box. There are no identifying marks on the magnetic toys.

As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

Presence of particulates in affected devices that can be deposited into breast tissue during use.

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

Due a design issue where the navigated array connection geometry is incorrect.

Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.

A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.

Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.

Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.