Philips recalls S8-3t Transducer Probes with specific model numbers for clarification on useful life labeling in medical ultrasound devices.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain S8-3t Transducer Probes to clarify labeling for the useful life of ultrasound transducers in the field. This recall does not involve safety hazards but aims to provide better labeling information for medical use.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard described; this is a labeling update to help users understand the expected lifespan of the transducers.
Medical professionals using Philips S8-3t Transducer Probes with the listed model numbers are affected. The recall targets specific units for labeling clarification, not safety risks.
Check for model numbers 989605420183, 989605431171, 989605420182, 989605420181, 989605379471 or UDI codes listed in the recall notice. The product is used in medical ultrasound devices.
Look for the model numbers or UDI codes listed in the recall notice to confirm if your transducer probe is affected.
No, this recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard.
No, the recall does not require stopping use; it is for labeling clarification to help users understand the expected lifespan of the transducers.
Check the model numbers or UDI codes listed in the recall notice. Affected units have specific model numbers or UDI codes provided in the record.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2398-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2398-2025 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.
