Philips recalls L17-5 Transducer Probes with specific model numbers for clarification on useful life labeling in medical ultrasound devices.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain L17-5 Transducer Probes to provide clearer labeling about their useful life in medical ultrasound applications. This recall focuses on labeling accuracy rather than safety risks.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. This is not a safety hazard but a labeling update to ensure proper usage duration.
Medical professionals using Philips L17-5 Transducer Probes with the listed model numbers are likely affected. Patients using these probes for ultrasound imaging may also be impacted by the labeling clarification.
Check for model numbers 8500-1662-01, 989605366373, 989605388061, 989605366371 or UDI codes starting with (01)00884838064614(21) followed by specific alphanumeric sequences listed in the recall.
Verify if your transducer probe has model numbers 8500-1662-01, 989605366373, 989605388061, or 989605366371.
Check for Unique Device Identification (UDI) codes starting with (01)00884838064614(21) followed by specific alphanumeric sequences listed in the recall.
Philips is recalling these transducers to provide clarification and labeling to define the useful life of ultrasound transducers in the field.
No, this recall is for labeling clarification to define useful life, not a safety hazard.
Check if your transducer has model numbers 8500-1662-01, 989605366373, 989605388061, 989605366371 or UDI codes starting with (01)00884838064614(21) followed by specific alphanumeric sequences listed in the recall.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2379-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2379-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
