FDA Enforcement Class III Ongoing

Transducer C10-3v Transducer Probe

Recall: Z-2401-2025 · Reported September 3, 2025

Enforcement

Recall Number
Z-2401-2025
Event ID
97217
Classification
Class III
Status
Ongoing
Product Type
Devices
Firm
Philips Ultrasound, Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
September 3, 2025
Initiation Date
July 3, 2025
Classification Date
August 22, 2025
Address
1 Echo Dr, Reedsville, PA, 17084-8603, United States

Description

Transducer C10-3v Transducer Probe

Reason

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

Code Info

Model No. N/A; UDI: N/A; Serial No. B2WXV7.

Distribution

US Nationwide distribution.

Quantity

171,322 units