Search Product Recalls

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.

NHTSAJun 4, 2025Nationwide• TRIPLE E RV

Azurion 7 M20 X-Ray (Philips Medical) – Gearbox Bolt Loosening (2025)

Potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose.

FDAJun 4, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

UROSKOP Omnia (Siemens Medical) – Frequency Inverter Fire Risk (2025)

A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.

FDAJun 4, 2025Nationwide• Siemens Medical Solutions USA, Inc

ADVIA 3-in-1 Control (Siemens Healthcare) – Platelet Value Error (2025)

Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.

FDAJun 4, 2025Nationwide• Siemens Healthcare Diagnostics, Inc.

Nissan Frontier (Nissan) – Display Unit Blank Screen (2025)

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."

NHTSAJun 4, 2025Nationwide• NISSAN

Zvu Anorectal Manometry Kit (Diversatek) – Expiration Date Mislabel (2025)

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.

FDAJun 4, 2025Nationwide• Diversatek Healthcare

UROSKOP Omnia Max (Siemens Medical) – Frequency Inverter Fire Risk (2025)

A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.

FDAJun 4, 2025Nationwide• Siemens Medical Solutions USA, Inc

Bornstein Frozen Shrimp Meat (Bornstein) – Listeria Contamination (2025)

Listeria

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.

Class IHigh

FDAJun 4, 2025Nationwide• Bornstein Seafoods Inc

SwabCap Disinfecting Cap (ICU Medical) – Seal Integrity Issue (2025)

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.

FDAJun 3, 2025Nationwide• ICU Medical, Inc.

BD Heyman Follower Straight Tip (C.R. Bard) – Catheter Size Incorrect (2025)

Cather packaging may contain the incorrect French size.

FDAJun 3, 2025Nationwide• C.R. Bard Inc

Mazda MX-5 (Mazda) – Stability Control System Problem (2025)

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."

NHTSAJun 3, 2025Nationwide• MAZDA

Ford Escape (Ford) – Cylinder Head Manufacturing Issue (2025)

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.

NHTSAJun 3, 2025Nationwide• FORD

Bard Urologist's Tray (C.R. Bard) – Catheter Size Incorrect (2025)

Cather packaging may contain the incorrect French size.

FDAJun 3, 2025Nationwide• C.R. Bard Inc

BD FACS Setup Beads (Becton Dickinson) – Spectral Overlap Error (2025)

Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.

FDAJun 3, 2025AZ, AR, CA +34 more• Becton, Dickinson and Company, BD Bio Sciences

Hamilton C6 (Hamilton Medical) – Circuit Board Mechanical Defect (2025)

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.

Very High

FDAJun 3, 2025Nationwide• Hamilton Medical AG Parc Industrial Vial 10 Domat/Ems Switzerland

Bravo CF Capsule Device (Given Imaging) – Adhesive Malfunction (2025)

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.

FDAJun 3, 2025Nationwide• Given Imaging Ltd. New Industrial Park

Ford Explorer (Ford) – Brake Caliper Bolt Issue (2025)

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.