Latest Product Recalls Today

Potential for attenuation degradation over time, decreasing the lifespan.

All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Potential for attenuation degradation over time, decreasing the lifespan.

All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.

All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments

Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous (steel) fittings instead of non-ferrous (brass) fittings on the magnet rear and if system is accessed to perform service while the magnet is ramped, the magnetic field could attract the ferrous fittings potentially resulting in personnel injury.

Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.

Forest River, Inc. (Forest River) is recalling certain 2026 Westbrook and Avenger travel trailers. The Federal Placard label may list an incorrect dry weight. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, “Tire Selection and Rims.” Incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2015-2022 Lexus RC, 2016-2020 GS, and 2022 IS vehicles. The low-pressure fuel pump inside the fuel tank may fail. Fuel pump failure can cause an engine stall, increasing the risk of a crash.

Bombardier Recreational Products, Inc. (BRP) is recalling certain 2025 Can-Am Origin electric motorcycles. A fatigue failure of the front brake caliper support may occur and result in inoperative front brakes. Front brake failure increases the risk of crash or injury.

Hyundai Motor America (Hyundai) is recalling certain 2023-2025 Hyundai Ioniq 6, 2023-2026 Genesis G90, 2024-2026 Hyundai Santa Fe, and Hyundai Santa Fe Hybrid vehicles. The driver and passenger seat belt anchors may detach. A detached seat belt anchor will not adequately restrain the seat occupant, increasing the risk of injury in a crash.

Greenpower Motor Company Inc. (Greenpower) is recalling certain 2020-2024 Nano Beast and 2021-2024 Beast school buses. The Cross View Mirror is designed to only view pedestrian around stopped buses. The label warning drivers not to use the mirror to view vehicular traffic may be missing. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility." Without a warning label, the driver may use the altered view to see other vehicles, increasing the risk of a crash.

Graco Children's Products Inc. (Graco) is recalling certain SnugRide Turn & Slide and Modes Nest Travel Systems with Snugride Turn & Slide infant child seats. Please refer to Graco's recall report for specific model information. The infant seat carrier may detach from the base in a crash. As such, these child seats and travel systems fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 213, "Child Restraint Systems." An infant seat carrier that detaches in a crash increases the risk of injury.

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2018 E 400 4MATIC Sedan, E 400 4MATIC Wagon, E 400 4MATIC Cabriolet, E 400 4MATIC Coupe, 2018-2020 Maybach S 560 4MATIC, S 560 4MATIC Coupe, S 450 4MATIC, 2019-2020 E 450 4MATIC Sedan, E 450 4MATIC Wagon, E 450 4MATIC Coupe, and E 450 4MATIC Cabriolet vehicles. The drive shaft universal joint may break, resulting in a sudden loss of drive power. A sudden loss of drive power increases the risk of a crash.

Autocar, LLC (Autocar) is recalling certain 2025-2026 ACX (Xpeditor) vehicles. The winter front cover may interfere with the forward collision warning (FCW) system. Interference may cause the FCW system to fail, increasing the risk of a crash.

This recall involves Tuymec Minoxidil Hair Growth Kit. The kits contain two black spray bottles with labels that read "Tuymec Minoxidil Hair Hair Growth", "Advanced Formula" and "5% Minoxidil with BIOTIN". The kits come in black cartons with white and silver lettering that include "Drug Facts" on the back, distributor information on one of its sides, three icons making product claims on its other side, and batch, manufacture and expiration dates on its bottom.

This recall involves TecFlox's topical solution bottles. The hair and beard growth serum comes in white plastic bottles fitted with a white nozzle and was sold in packs of four bottles. "TecFlox Minoxidil Topical Solution" is printed on the bottle's label and the manufacture date "MFD 2025.8.25" on the underside of the bottle.

This recall involves Sangohe-branded adult portable bed rails models 504E and 504Q. Model 504E bed rail comes in black, measures 23 inches wide by 35 inches tall, and weighs nine pounds. The model number "504E" can be found on the outer packaging box, on the product label/sticker attached to the bed rail, and on the first page of the instruction manual. Model 504Q bed rail comes in black, measures 28.5 inches wide by 43.3 inches tall, and weighs nine pounds. The model number "504Q" can be found on the outer packaging box, on the product label/sticker attached to the bed rail, and on the first page of the instruction manual.

This recall involves Ocun Condor HMS Triple Carabiners sold in dark gray and blue. The carabiners have an independent internal wire gate for belaying and rappelling and a triple locking action gate. The affected carabiners have the following batch numbers 24003xx, 24004xx, 24010xx, 24023xx, 24024xx, 24025xx, 25005xx, 25006xx. The batch number is found on the spine of the carabiner.

This recall involves battery chargers, model T400, sold under the brand names "HTRC" and "Haisito." The recalled chargers are black with a touch screen, and the model number T400 is printed on the front. Some units have the brand name "HTRC" printed on the front, while other units do not have a visible brand name. Units without a visible brand name may still have the model number "T400" printed on the front. The brand name "Haisito" may not be printed on the product but may be located on the purchase receipt.

This recall involves Gavoyeat Halloween Light-Up Rings Party Favors, model number 43398-68657. "B07GF8VD7N" appears on the back of packaging. The light-up rings come with 50 multi-colored party favors that light up and each includes three preinstalled button cell batteries. The batteries are visible through the inner clear casing. The light-up rings have "Holiday Party Favors LED Light Up Ring" printed on the back of the package.