S4-1 Lumify Transducer Probe
FDA Recall Z-2392-2025 · Posted 2025-08-22
Recalling FirmPhilips Ultrasound, Inc
Recall StatusOpen, Classified
Product CodeIYN
Date Initiated2025-07-03
Product Quantity171,322 units
Reason for Recall
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Firm Action
An URGENT Medical Device Correction Notice, dated 7/3/25, was mailed to consignees. This notice instructs consignees to locate all Philips Ultrasound transducers in their facility and enter their serial numbers into https://www.transducer.philips.com to obtain the manufacturing certificate for each of their devices. This certificate should be retained with its system documentation. Using the manufacturing certificate consignees are to calculate the useful life of their device. The expected useful life for Transesophageal transducers, X-Matrix transducers, and Lumify transducers is 5 years; The expected useful life for Endocavity transducers and Transcutaneous transducers is 7 years. If a transducer has exceeded its useful life, consignees are instructed to conduct transducer performance tests or contact Philips for guidance. Consignees are asked to complete and return the provided response form and circulate the recall notification to device users for their awareness. Consignees with any questions can contact Philips Customer Care Solutions Center at 1-800-722-9377.
Root Cause
Device Design
Distribution Pattern
US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
K223771Lumify Diagnostic Ultrasound SystemPhilips Ultrasound · 2023-05-04K203406Lumify Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2021-02-23K201012EPIQ Diagnostic Ultrasound System Series, Affiniti Diagnostic Ultrasound System Series, CX50 Diagnostic Ultrasound System, Sparq Diagnostic Ultrasound System, Lumify Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2020-05-01K192226Lumify Diagnostic Ultrasound SystemPhilips Health Care · 2019-09-06K162549Lumify Ultrasound SystemPhilips Health Care · 2016-10-03
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.