Philips recalls S7-3t Transducer Probes with specific model numbers for labeling clarification on useful life in medical ultrasound. 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 S7-3t Transducer Probes to clarify their useful life in medical ultrasound 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 a labeling update to help users understand how long the transducers are expected to function before needing replacement.
Healthcare professionals using Philips S7-3t Transducer Probes with the listed model numbers may need updated labeling for accurate use duration. No safety risk is involved.
Check for model numbers 989605406772, 989605439232, 21781A, 989606708921, 989605406771, 989605414122, or UDI codes starting with (01)00884838061439(21) followed by specific sequences listed in the recall.
Review the model numbers listed in the recall to determine if your transducer is affected.
Philips will provide updated labeling to clarify the useful life of the transducers in medical use.
No, this recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety risk involved.
No, the recall does not require stopping use. This is a labeling update for accurate use duration.
Check the model numbers listed in the recall or the UDI codes starting with (01)00884838061439(21) followed by specific sequences.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2395-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2395-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
