Medical DeviceJul 9, 2025
Philips eL18-4 EMT Transducer recall — FDA Z-2053-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Recall history in this database
Classification mix: Class II: 22.
Medical DeviceJul 9, 2025
Philips C9-5EC Transducer recall — FDA Z-2051-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips eL18-4 Transducer recall — FDA Z-2052-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips C5-2 Transducer recall — FDA Z-2050-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips L12-3 Transducer recall — FDA Z-2054-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips X6-1 Transducer recall — FDA Z-2065-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips X8-2t Transducer recall — FDA Z-2067-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips V6-2 Transducer recall — FDA Z-2062-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips S5-1 Transducer recall — FDA Z-2058-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips S7-2 Transducer recall — FDA Z-2059-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips 3D9-3v Transducer recall — FDA Z-2048-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips X7-2t Transducer recall — FDA Z-2066-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips X5-1 Transducer recall — FDA Z-2064-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips S8-3t Transducer recall — FDA Z-2061-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips XL14-3 Transducer recall — FDA Z-2068-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips C5-1 Transducer recall — FDA Z-2049-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips L12-4 Transducer recall — FDA Z-2055-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips VL13-5 Transducer recall — FDA Z-2063-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips L8-4 Transducer recall — FDA Z-2056-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips L9-3 Transducer recall — FDA Z-2057-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips S7-3t Transducer recall — FDA Z-2060-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceMay 15, 2024
Philips Ultrasound 5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 recall — FDA Z-1757-2024
Ultrasound system with: 1) transesophageal echocardiography transducer (TEE) connected/not selected 2) 1, 2 non-TEE connected 3) Imaging with non-TEE 4) Selected/not selected imaging…
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Philips Ultrasound, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.