Philips Ultrasound, Inc recalls Philips S8-3t Transducer.
- Recall date
- May 28, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2061-2025
- FDA classification
- Class II
- Brand / firm
- Philips Ultrasound, Inc
- Sold / distributed
- 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…
Why it was recalled
Ultrasound transducer devices were refurbished beyond their useful life.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Philips S8-3t Transducer.
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