PlainRecalls
FDA Devices Moderate Class II Ongoing

Philips C5-2 Transducer.

Reported: July 9, 2025 Initiated: May 28, 2025 #Z-2050-2025

Product Description

Philips C5-2 Transducer.

Reason for Recall

Ultrasound transducer devices were refurbished beyond their useful life.

Details

Recalling Firm
Philips Ultrasound, Inc
Units Affected
5,230 units
Distribution
Domestic: Nationwide Distribution; Foreign: Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Luxembourg, Malaysia, Mexico, Morocco, Netherlands, New Caledonia, New Zealand, Nicaragua, Oman, Philippines, Poland, Portugal, Romania, Russian Fed., Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Thailand, T¿rkiye, United Kingdom, United Arab Emirates, Venezuela, Vietnam.
Location
Reedsville, PA

Frequently Asked Questions

What product was recalled?
Philips C5-2 Transducer.. Recalled by Philips Ultrasound, Inc. Units affected: 5,230 units.
Why was this product recalled?
Ultrasound transducer devices were refurbished beyond their useful life.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 9, 2025. Severity: Moderate. Recall number: Z-2050-2025.