Philips recalls S4-1 Transducer Probes with specific model and serial numbers for labeling clarification to define useful life in field use. No safety hazard exists; this is a labeling update for product longevity.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain S4-1 Transducer Probes to update labeling about their expected useful life in field use. This recall does not involve a safety hazard but aims to provide clearer information for proper maintenance and usage.
The recall addresses a need for clearer labeling to define the useful life of ultrasound transducers in the field. This helps users understand how long the probes should be expected to function before needing replacement. There is no safety hazard involved.
Users of Philips S4-1 Transducer Probes with the listed model and serial numbers are affected. Medical professionals using these probes for ultrasound imaging are most at risk due to potential confusion about product longevity.
Check the model numbers on the probe: 989605389271, 989605389272, 989605364993. Also look for the serial numbers listed in the recall notice, such as B30VBN or B1GPT4.
Identify the model numbers (989605389271, 989605389272, 989605364993) and serial numbers (e.g., B30VBN, B1GPT4) on your S4-1 Transducer Probe.
No, the recall is for labeling clarification to define useful life in field use, not a safety hazard.
No, the recall does not require stopping use; it's a labeling update for product longevity.
Check the model numbers (989605389271, 989605389272, 989605364993) and serial numbers (e.g., B30VBN, B1GPT4) on your probe.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2391-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2391-2025 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.
