Philips recalls specific C8-5 Transducer Probe models for labeling clarification to define useful life in the field. No safety risk, but updated labeling required for proper use.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain C8-5 Transducer Probes to update labeling that defines their useful life in the field. This is a labeling clarification, not a safety hazard. Users should check their model numbers to see if they are affected.
This recall is for labeling clarification to define the useful life of the transducers in the field. There is no safety hazard or risk of injury; it's a labeling update to ensure proper usage and maintenance.
Users of Philips C8-5 Transducer Probes with the model numbers listed in the recall notice are affected. Healthcare professionals using these probes for ultrasound imaging are most at risk.
Check if your C8-5 Transducer Probe has one of the model numbers listed in the recall notice (e.g., 989605391922, 989605438441, etc.). The recall includes specific UDI codes as well.
Verify your C8-5 Transducer Probe's model number against the list provided in 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.
No action is required. This is a labeling update to ensure proper use and maintenance.
Check your model number against the list of affected models provided in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2359-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2359-2025 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.
