Philips recalls S5-2 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 S5-2 Transducer Probes to clarify their useful life in the field through proper labeling. This is not a safety hazard but a labeling update to help users understand the product's expected lifespan.
The recall is for labeling clarification to define the useful life of the transducers in the field. This is not a safety hazard but a labeling update to help users understand the product's expected lifespan.
Users of Philips S5-2 Transducer Probes with the listed model numbers may need updated labeling for field use. No safety risk is involved.
Check your S5-2 Transducer Probe for model numbers listed in the recall (e.g., 989605412082, 989605440682). Also look for the UDI codes provided in the recall notice.
Identify your S5-2 Transducer Probe model number from the list provided in the recall notice.
Ensure the product has updated labeling that defines the useful life in the field as per the recall notice.
No, this recall is for labeling clarification to define the useful life of the transducers in the field. There is no safety risk involved.
No, you do not need to stop using it. This is a labeling update for field use, not a safety hazard.
Check your model number against the list provided in the recall notice (e.g., 989605412082, 989605440682). Also look for the UDI codes listed in the recall.
We’ve drafted a message you can send Philips Ultrasound to request your refund or repair — edit it as you like.
Subject: Recall Z-2394-2025 — Philips Ultrasound Philips Ultrasound Hello, I own a Philips Ultrasound that is covered by recall Z-2394-2025 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.
