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All product recalls affecting North Dakota.
Includes nationwide recalls (tagged “Nationwide”) and recalls with North Dakota in the distribution area.
This recall involves the BowFlex branded Model 552, 52.5 LB Adjustable Dumbbells and Model 1090, 90 LB Adjustable Dumbbells. The dumbbells were sold in pairs and single units in the color black and include handles, weight plates and a molded plastic tray. The model 552 dumbbells adjust from 5 to 52.5 pounds and the model 1090 adjusts from 10 to 90 pounds using manual adjustment knobs while the weights are nested in the base. The model and serial number are printed on a sticker located on the bottom of the molded plastic tray. The following model and serial number ranges are included in this recall. Model Number Serial Number Range BowFlex 552 Adjustable Dumbbells 00182M243902233 - 00182M243902592 00182MAG220200463C - 00182MAG221204535C 00182SFE213414844C - 00182SFE234002231C 100182M242800001 - 100182M250201440 100182MAG20431227C - 100182MAG233500372 100182P244100067 - 100182P244602976 100182SFE213709609 - 100182SFE235206276 100748M243200001 - 100748M244300252 100748MAG222400734 - 100748MAG23500660 100748P242900001 - 100748P245205632 100748SFE220908785 - 100748SFE233513811 X00748MAG233003670 - X00748MAG233003672 X00748SFE233202493 - X00748SFE233203161 Z00748MAG233003670 BowFlex 1090 Adjustable Dumbbells 4551MAG21452813 - 4551MAG23350381 4551SFE23320001 - 4551SFE23501949 BowFlex Inc. filed for bankruptcy protection in March 2024. Johnson Health Tech Trading has agreed to provide a remedy for the 552 and 1090 adjustable dumbbells sold by BowFlex Inc., (formerly Nautilus Inc.), prior to May 2024 as a part of this recall.
High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
An incoming complaint reported that the expiration date on the kit box label and Certificate of Analysis (CoA) exceeded the shelf life of the standards and control solutions in the kit by 2 months (i.e., 2026-03-31 instead of 2026-01-31). The expiration dates on the bottle labels were correct (i.e., 2026-01-31).
Triple E Recreational Vehicles (Triple E) is recalling certain 2025 Wonder W24RTB, W24RL, W24MBL, Unity U24RL, U24TB, U24MBL, U24MB, U24FX, and U24CB motorhomes. The insulation on the inverter wiring may have been incorrectly installed, allowing the wiring to overheat.
Potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose.
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
Nissan North America, Inc. (Nissan) is recalling certain 2025 Frontier and Kicks vehicles. The center information display unit may display a blank screen when shifted into reverse. As such, these vehicles fail to comply with Federal Motor Vehicle Safety Standard (FMVSS) number 111, "Rear Visibility."
Anorectal manometry procedure kit outer kit label is mislabeled with an incorrect expiration date; the manufacturing date was used in place of the expiration date. All inner labels on kit components display the correct expiration date.
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
The recall was the result of the firm's routine sampling program and Listeria monocytogenes was detected in an in-process shrimp sample in a food production environment.
Due to a manufacturing issue, disinfecting cap for needle-free connectors may have an incomplete seal between the foil lid and plastic container, which may result in isopropyl alcohol evaporation from the sponge, which may result in inadequate disinfection.
Cather packaging may contain the incorrect French size.
Mazda North American Operations (Mazda) is recalling certain 2024-2025 Mazda MX-5 vehicles. The Traction Control System (TCS) and Dynamic Stability Control (DSC) indicator light may fail to illuminate as intended due to a software error. As such, these vehicles fail to conform to Federal Motor Vehicle Safety Standard number 126, "Electronic Stability Control Systems."
Ford Motor Company (Ford) is recalling certain 2023-2025 Escape, and 2025 Bronco Sport vehicles. The cylinder head may have been improperly manufactured, which can cause the ball plugs to fail, resulting in an oil leak.
Cather packaging may contain the incorrect French size.
A mechanical defect on a printed circuit board (PCB) as a result of PCB separating process. This defect might cause the ventilator to either fail at startup (no patient involvement) or during the use of the device enter ambient state, resulting in an interruption of ventilation.
It has been determined that misapplied adhesive on the Bravo CF capsule delivery device may lead to its malfunction. Specifically, the misapplied adhesive may prevent the capsule from attaching to the patient's esophagus or detaching from the delivery device.
Ford Motor Company (Ford) is recalling certain 2025 Explorer vehicles. The bolts securing the front brake caliper may not be tightened properly, which can result in a loss of front brake function and possible wheel damage.