Philips recalls L12-4 Lumify Transducer Probes with specific model numbers for labeling clarification on useful life in the field. No safety risk, but updated labeling required.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain L12-4 Lumify Transducer Probes to clarify their useful life in the field through proper labeling. This is a labeling update, not a safety hazard.
The recall is for labeling clarification on the useful life of the transducers in the field. There is no safety hazard or risk of injury.
Users of Philips L12-4 Lumify Transducer Probes with the listed model numbers may need updated labeling for field use duration.
Check your L12-4 Lumify Transducer Probe for model numbers: 989605434813, 989605451171, 989605434812, 989605477121, 989605434811, or UDI codes listed in the recall notice.
Look for model numbers on the transducer probe: 989605434813, 989605451171, 989605434812, 989605477121, 989605434811, or UDI codes in the recall list.
No, this recall is for labeling clarification on the useful life of the transducers in the field. There is no safety risk.
No, you can continue using it normally. This is a labeling update, not a safety issue.
No action is needed beyond checking the model numbers to confirm if it's affected. Philips is providing updated labeling information.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2374-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2374-2025 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.
