Philips recalls 7.5MHz Endo Transducer Probe for labeling clarification on useful life in medical use. No immediate safety risk but requires updated labeling.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling its 7.5MHz Endo Transducer Probe to clarify labeling for useful life in medical applications. This is a labeling update, not a safety hazard.
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 the probe for ultrasound imaging. The risk is minimal as it's a labeling clarification for useful life.
Check for the 7.5MHz Endo Transducer Probe with serial number F00262. The product has no unique identifier (UDI).
Check the product label for updated useful life information as per Philips' clarification.
No, this recall is for labeling clarification on useful life in medical use, not a safety hazard.
No action is needed beyond reviewing the updated labeling for useful life information.
The product has serial number F00262, but no unique identifier (UDI).
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2348-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2348-2025 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.
