Philips Ultrasound, Inc: Device Recall

Recall #Z-2385-2025 · 07/03/2025

Class III: Low Risk

Recall Details

Recall Number: Z-2385-2025
Classification: Class III
Product Type: Device
Recalling Firm: Philips Ultrasound, Inc
Status: Ongoing
Date Initiated: 07/03/2025
Location: Reedsville, PA, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 171,322 units

Reason for Recall

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

Product Description

Mini Multi TEE Transducer Probe

Distribution Pattern

US Nationwide distribution.

Other Recalls by Philips Ultrasound, Inc

Class III: Low Risk 07/03/2025

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III: Low Risk 07/03/2025

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III: Low Risk 07/03/2025

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III: Low Risk 07/03/2025

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III: Low Risk 07/03/2025

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

View all recalls by Philips Ultrasound, Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.