Latest Product Recalls Today

This recall involves Workbless-branded pressure washers, models WB0301 and WB0302. Model WB0301 is green and black and measures about 27.24 inches high, 10.83 inches wide and 8.39 inches deep. "WORKBLESS"," WB0301" and "ELECTRIC PRESSURE WASHER" are printed on a label on the back of the pressure washer. Model WB0302 is also green and black and measures about 29.57 inches high, 14.69 inches wide and 10.94 inches deep. "WORKBLESS", "WB0302" and "HEAVY DUTY ELECTRIC PRESSURE WASHER" are printed on a label on the back of the pressure washer. Both models came with four quick connect nozzles and a foam cannon.

This recall involves ventilation fans in ClassMate cooling and air source heat pumps and SchoolMate water/ground source heat pumps that supply heating, cooling and high indoor air quality in classrooms and schools in the following models: Model Ventilation Configuration (Digit 9) CMD C, D, or E CMP C, D, or E SMG H, J, K, N, or P SMW H, J, K, N, or P CMS H, J, K, N, or P The brand name Airedale is located on a sticker on the front of the unit. The model name and serial number are found on the serial plate on the underside of the control unit.

This recall involves 2021, 2022, 2023 and 2024 off-road motorcycles. The GASGAS off-road motorcycles are red with the white GASGAS logo on both sides of the shrouds. The Husqvarna motorcycles are white, blue and yellow with the Husqvarna logo on both sides of the shrouds. The VIN and number are located on the right side of the steering head. Recalled 2021, 2022, 2023 and 2024 Off Road Motorcycles Model Year Husqvarna Models 2022 FE 350 2022 FE 501 2022 TE 150i 2022 TE 250i 2022 TE 300i 2023 TE 150 2023 TE 250 2023 TE 300 2023 TE 300 Heritage 2023 FX 350 Heritage 2023 FX 350 2023 FE 450 2023 FE 450 Heritage 2023 FX 450 2023 TX 300 2023 TX 300 Heritage 2024 TE 150 2024 TE 250 2024 TE 300 2024 FE 350w 2024 FE 450 2024 FE 501w Model Year GASGAS Model 2021 EC 300 2022 EC 250 2022 EC 300 2023 EC 250 2023 EC 300 2023 EX 250 2023 EX 250F 2023 EX 300 2023 EX 350F 2023 EX 450F 2023 MC 125 2023 MC 250 2023 MC 250F 2023 MC 350F 2023 MC 450F 2024 MC 125 2024 MC 250 2024 MC 250F 2024 MC 350F 2024 MC 450F 2024 EC 250 2024 EC 300 2024 EC 450F 2024 EX 250 2024 EX 250F 2024 EX 300 2024 EX 350F 2024 EX 450F 2024 EW 500F

This recall involves Koorlian branded mattresses. The mattresses are 10 inches thick and were sold in a Twin XL size. They have a white top and blue sides and were sold compressed in a box. "Dreams Bedding Technology PTE LTD" the manufacture date and prototype ID "KY15Q290" are printed on a sewn-in white label located on one side of the mattress.

This recall involves JINHEZO Mini Waterproof LED Tea Lights. The circular tea lights are clear with a white base and are about 1" in diameter and 1.14" tall. They come in a pack of 24 lights with 48 coin-cell batteries (two per light).

This recall involves Goal Zero's YETI 3000X power stations. The silver and black portable power stations measure about 24.4 inches high, 18.5 inches wide and 22.3 inches deep, and weigh about 92 pounds. The power stations have yellow handles and a digital display at the front with electrical ports. They sit on a rolling cart with two built-in wheels and a telescoping handle. The Goal Zero logo is printed on the front bar of the cart and on a nameplate located on the underside of the station's lid along with "YETI 3000X".

This recall involves the CCM Hybrid Hockey Visors, style FMHVR and replacement visor accessories, style ACCHVR. The recalled FMHVR Hybrid Visors are marked "HVR" at the top of the metal plate (above "CCM" in red). Recalled FMHVR visors have serial numbers beginning with "M/L" or "S/M." The recalled ACCHVR Replacement Visor accessory has serial numbers beginning with "SR". The serial number is printed at the top corner on the right- hand-side metal plate where HVR - CCM are written, inside of the visors, engraved into the polycarbonate. The following visor and visor accessories are included in the recall. Recalled Visors and Visor Accessories: S/M FMHVR SR CCM CAG Visor Black Chrome S/M M/L FMHVR SR CCM CAG Visor Black Chrome M/L M/L ACCHVR CONTAINS REPLACEMENT VISOR(1) + SIDE CLIPS(2) + SPACERS(2) + SCRFEWS(2) S/M ACCHVR CONTAINS REPLACEMENT VISOR(1) + SIDE CLIPS(2) + SPACERS(2) + SCRFEWS(2)

Avride Inc. (Avride) is recalling certain Automated Driving Systems (ADS) equipped with software versions prior to RC-01-05. The ADS software may direct the vehicle to change lanes, merge, or veer left or right without yielding or maintaining a safe distance from other vehicles. Unexpected vehicle movement may increase the risk of a crash.

E-One Incorporated (E-One) is recalling certain 2026 Cyclone 2, 2025-2026 Cyclone, and Typhoon fire trucks. The hydraulic valve may become inoperative, preventing the outriggers from being extended or retracted. The inability to extend or retract the outriggers can delay emergency response, increasing the risk of injury.

Possible Salmonella Enteritidis

Label declares cream and cheese, but Milk is not declared

Undeclared Red #40.

Undeclared peanuts

Possible Salmonella Enteritidis

Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss of geometry movements that may lead to delay of therapy and procedural complications

Due to increase in false negative results

There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare provider.

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.

The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or inappropriate monitoring of renal disease in intended users.

There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the issue could cause bone compression or difficulty during installation in situations where there is sufficient bone volume

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as the plateau cannot be inserted and an alternative product would be needed. If the incorrect plateau were to be implanted, this is associated with increased risk of wear, which could result in a reduced standing time of the implant.

Products may not have received adequate sterilization processing.