Class II

Medical Device Recall: Philips S7-2 Transducer.

Philips Ultrasound, Inc · May 28, 2025

Reason for Recall

Ultrasound transducer devices were refurbished beyond their useful life.

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.

States Affected

NATIONWIDE

Quantity Affected

5,230 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2059-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Philips Ultrasound, Inc Medical Device Recall: Philips S7-2 Transducer. | SafeCheck