Philips recalls eL18-4 Transducer Probes with specific model numbers for clarification on useful life in field use. No immediate safety risk, but labeling updates are needed.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain eL18-4 Transducer Probes to clarify their useful life in field use. This is a labeling update, not a safety hazard. No action is needed for safety, but the product may need re-labeling.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard described.
Users of Philips eL18-4 Transducer Probes with the listed model numbers may need updated labeling for field use duration. This is not a safety issue.
Check your eL18-4 Transducer Probe for model numbers: 989605431531, 989605456291, 989605391092, 989605412062, 989605409562, or UDI codes starting with (01)00884838070806(21) followed by specific characters.
Look for model numbers on the probe: 989605431531, 989605456291, 989605391092, 989605412062, 989605409562, or UDI codes starting with (01)00884838070806(21).
No, this recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard.
No action is needed for safety, but the product may require updated labeling for field use duration.
Affected models include 989605431531, 989605456291, 989605391092, 989605412062, 989605409562, and UDI codes starting with (01)00884838070806(21).
We’ve drafted a message you can send Philips Ultrasound to request your refund or repair — edit it as you like.
Subject: Recall Z-2369-2025 — Philips Ultrasound Philips Ultrasound Hello, I own a Philips Ultrasound that is covered by recall Z-2369-2025 from Philips Ultrasound. 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.
