Philips recalls L18-5 Transducer Probes with specific model numbers for labeling clarification on useful life in medical ultrasound. No safety risk, but updated labeling required for field use.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain L18-5 Transducer Probes to update labeling about their useful life in medical ultrasound applications. This is a labeling clarification, not a safety hazard.
The recall is for labeling clarification to define the useful life of the transducers in field use. There is no safety hazard or risk of injury.
Medical ultrasound users who own or use the recalled L18-5 Transducer Probes with the listed model numbers. The recall does not pose a safety risk.
Check if your L18-5 Transducer Probe has model numbers listed in the detailed UDI codes provided. The recall covers specific model numbers with unique identifiers.
Review the model numbers on your transducer probe to see if they match the listed UDI codes in the recall.
No, this recall is for labeling clarification to define the useful life of the transducers in field use. There is no safety risk.
No, the recall does not require stopping use. The transducers can continue to be used with updated labeling.
Check the model numbers on your transducer against the detailed UDI codes 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-2380-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2380-2025 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.
