Philips recalls specific L11-3 Transducer Probes for labeling clarification on useful life in field use. No safety hazard exists; this is a labeling update for better product longevity.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain L11-3 Transducer Probes to update labeling about their expected useful life in field use. This is not a safety hazard but helps users understand how long the probes should be expected to function properly.
The recall involves updating labeling to clarify the useful life of ultrasound transducers in real-world use. This is not a safety hazard but helps users understand how long the probes should be expected to function properly before needing replacement.
Users of Philips L11-3 Transducer Probes with the listed model and serial numbers are affected. Healthcare professionals using these probes for medical imaging are most at risk of confusion about expected lifespan.
Check your L11-3 Transducer Probe for model numbers 989605388251, 989605400511, 989605400513, or 989605440762. Also look for serial numbers listed in the recall notice.
Verify your transducer probe's model and serial numbers against the list provided in the recall notice.
No, this recall is for labeling clarification on useful life in field use, not a safety hazard.
No, you can continue using it normally as this is a labeling update for better product longevity.
Check the model numbers 989605388251, 989605400511, 989605400513, or 989605440762, and serial numbers listed in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2371-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2371-2025 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.
