Latest Product Recalls Today

Forest River Bus, LLC (Forest River Bus) is recalling certain 2026 Collin Bus transit buses. The body panel joint adhesive may have been applied to the incorrect location, causing the panels to separate. As such these vehicle fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 221, "School Bus Body Joint Strength." Separated body panels can reduce structural integrity, increasing the risk of injury in a crash.

Forest River Bus, LLC (Forest River Bus) is recalling certain 2026 Collins Bus school buses. The body panel joint adhesive may have been applied to the incorrect location, causing the panels to separate. As such these vehicle fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 221, "School Bus Body Joint Strength." Separated body panels can reduce structural integrity, increasing the risk of injury in a crash.

Grand Design RV, LLC (Grand Design) is recalling certain 2025-2026 Lineage recreational vehicles. The adhesive securing the solar panels to the roof may fail, allowing the solar panel to detach. A detached solar panel can become a road hazard for other vehicles, increasing the risk of a crash.

General Motors, LLC (GM) is recalling certain 2024-2025 Chevrolet Blazer EV vehicles that may have been repaired incorrectly under recall 25V433. The rear parking brake wiring harness may become damaged or corroded, resulting in unintended activation of the parking brake or loss of the parking brake function. Unintended activation of the parking brake while driving increases the risk of a crash. Loss of the parking brake function while parked can result in a rollaway, increasing the risk of a crash.

This recall involves the Yetonamr 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, silicone pull string "tentacles" of various colors running through the ball. There are also three free-spinning rings and soft push buttons on the disc. "Model no. 688-59" is printed on the product packaging.

This recall involves Vndueey Magnetic Men toy sets. The toy sets consist of 10 flexible, stick figures in red, orange, pink, yellow, blue, bright red, bright green and transparent. Each stick figure has four small magnets, one in each hand and foot.

This recall involves Topkay Torch Lighters. The metal lighters are black and come in a two-pack. "Honest" is printed on the front of lighter.

This recall involves Mikario Trading's 5-in-1 baby gyms. The recalled baby gyms convert from an activity center to a tummy-time pillow mat. They were sold in pink and have a toy bar, six detachable plush toys and a set of milestone cards. "Baby Gym" and "Item No.: CBPBG-PIN" are printed on a label stitched to the product on the edge of the mat at the bottom.

This recall involves Iristar Minoxidil Spray Bottles, 5% minoxidil with biotin for hair and beard growth. The sprays come in black plastic bottles with navy blue labels and white highlights with a spray cap. The bottles and outer packaging are labeled "Iristar" and "Minoxidil Spray" on the front and ingredients and directions for use are found on the back.

This recall involves Gagaku-branded ice cream shop toy playsets. The recalled toy set includes 16 wooden pieces: a cash register, three ice cream cones, six scoops of ice cream, four popsicles, and two cupcakes in varying colors or "flavors." It also comes with one plastic credit card, five plastic dollar bills, one plastic menu and a two-level pink display box labeled "ICE-CREAM" on the front, with a black sign on the side. "GAGAKU" and "Model: KABI-0176 G062401IC" are printed on a label on the underside of the toy.

This recall involves Based Online Fidget Magnet Ball Toy Sets. Each set includes four textured, silicone-covered magnet balls in white, yellow, blue and purple. Each ball is about 1.24 inches in diameter. The magnet toys come in a black fabric zippered case. There are no identifying marks on the magnet toys.

This recall involves Cumbor-branded retractable safety gates. The recalled gates have a metal frame and a mesh screen that measures about 34 inches high with an adjustable width up to 55 inches. The gates were sold in black, gray, and white and came with one or more suction cups. "Model Name: Retractable Safety Gate," "Model Number: S5V2" and "Cohort Information: A202504S5V2A001" are printed on a label sewn to the mesh screen.

Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.

increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.

Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups. n certain cases, the system may indicate the patient as correctly positioned at the isocenter, even when the isocenter is positioned outside of the indicated tolerance.

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.