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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 26 Results
510(K) Number: K163120
 
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FDA Recall
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Philips VL13-5 Transducer. 2 07/02/2025 Philips Ultrasound, Inc
Philips S7-3t Transducer. 2 07/02/2025 Philips Ultrasound, Inc
Philips L12-4 Transducer. 2 07/02/2025 Philips Ultrasound, Inc
Philips 3D9-3v Transducer. 2 07/02/2025 Philips Ultrasound, Inc
Philips X8-2t Transducer. 2 07/02/2025 Philips Ultrasound, Inc
Philips X6-1 Transducer. 2 07/02/2025 Philips Ultrasound, Inc
Philips X5-1 Transducer. 2 07/02/2025 Philips Ultrasound, Inc
D2TCD Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
L18-5 Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
Mini Multi TEE Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
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