Latest Product Recalls Today

This recall involves the Flaunt MagSafe Battery Charger power banks with model number E33A. "FLAUNT" is engraved on the front right side of the power bank and there is a small circular button in the bottom center of the front side of the power bank. The back label of the unit is marked "FLAUNT" and "Model: E33A". The power banks were sold in melon, black, lavender and white. The chargers measure 3 by 2 by 0.25 inches and weigh around 3.2 ounces.

This recall includes the stainless-steel Cuisinart Propel+ Four Burner 3-in-1 Gas Grill, featuring a griddle, a stove top burner and a pizza oven with tempered glass located on top of the lid of the grill. The model number CGG-6331 can be found on the label on the inside of the right-hand metal door, along with the serial number.

This recall involves BBRKIN and MouTec Biometric Gun Safes with model number QHXP029B. The gray steel safes are used to store firearms and valuables. The safes measure about 14 inches by 12 inches by 57 inches, have one shelf and can store approximately five firearms. The recalled safes have the following serial number range: SQC200034980 - SQC202319171. The serial number is on a label on the lower right corner of the front of the safes. The brand name "MouTec" or "BBRKIN" is on the upper right corner of the front of the safes.

This recall involves Insignia gas ranges with model numbers NS-RGFGSS1 and NS-RGFCGS2. The recalled ranges are stainless steel with five front-knobs on the oven with the "Insignia" label on the bottom of the oven door. A label with the model number can be found on the inside of the range's bottom drawer.

Volvo Trucks North America (Volvo Trucks) is recalling certain 2026 VOLVO VHD, VNL (4), VNR (4), VN, and VAH vehicles. The steering knuckles may have been manufactured with insufficiently tightened steering arms. A loose steering arm can result in a loss of vehicle steering control, increasing the risk of a crash.

Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2026 Lexus TX Plug-In Hybrid, TX Hybrid, TX, Toyota Grand Highlander Hybrid, and Grand Highlander vehicles. The rear axle carriers may have been manufactured with insufficient material strength and could break. A broken rear axle carrier can cause a sudden loss of vehicle stability and control, increasing the risk of a crash.

Forest River, Inc. (Forest River) is recalling certain 2026-2027 Wildwood and Salem travel trailers. The Federal Placard may have the incorrect Gross Vehicle Weight Rating (GVWR). As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - Other than Passenger Cars." Referencing the incorrect GVWR may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

PACCAR Incorporated (PACCAR) is recalling certain 2026-2027 Peterbilt 579 and 2027 Kenworth T680 tractors. The trailer air connection quick release (QR) valve in the air brake system may have been incorrectly installed, which can cause the trailer to become unstable after the driver applies the brakes. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems." An incorrectly installed quick release valve that does not function properly can increase the risk of a crash.

KTM North America, Inc. (KTM) is recalling certain 2022-2024 Husqvarna FE 501S, Husqvarna FE 350S, 2024 GasGas ES 350, and GasGas ES 500 motorcycles. During backwards rolling, the brake caliper may crack near the primary pin casting, which may cause the caliper to break when riding. Cracks or breaks in the rear brake caliper can reduce braking ability, increasing the risk of a crash.

BMW of North America, LLC (BMW) is recalling certain 2018-2020 530e xDrive, 2017-2019 740Le xDrive, 2018-2020 530e iPerformance, 2016-2018 330e iPerformance vehicles. The engine starter relay may corrode, causing the relay to overheat and short circuit. A short circuit in the starter relay may increase the risk of a fire.

Potential contamination with plastic material

Product may be contaminated with Clostridium botulinum.

Dietary supplement product Ocular Plus contains undeclared Yellow#5.

Dietary supplement product Vista MAX contains undeclared Yellow#5.

Undeclared peanuts.

Product may be contaminated with Salmonella Typhimurium

Undeclared allergen (milk) and process deviation (product not held under refrigeration as required)

Potential contamination with plastic material

There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.

Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delivery due to loss of insulin to an external leak. If insulin is not delivered properly, users may experience high blood glucose levels due to under-delivery of insulin. In the most severe cases, prolonged and persistent high blood glucose levels can lead to diabetic ketoacidosis (DKA), hyperglycemic hyperosmolar syndrome (HHS), or even death.