Philips recalls V9-2 Transducer Probes with specific model numbers for labeling clarification on useful life in medical ultrasound. No safety hazard exists; this is a labeling update.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain V9-2 Transducer Probes to clarify their useful life in the field through labeling. This is not a safety hazard but a labeling update to help users understand how long these probes should be used before replacement.
This recall is for labeling clarification only. Philips is updating the useful life information for these transducers to help users understand when they should be replaced. There is no safety hazard or risk of injury.
Medical professionals using Philips V9-2 Transducer Probes with the listed model numbers. No safety risk exists.
Check your V9-2 Transducer Probe for model numbers: 989605466201, 989606717071, 989605492481, 989605456291, or UDI codes starting with (01)00884838...
Look for model numbers on the probe: 989605466201, 989606717071, 989605492481, 989605456291, or UDI codes starting with (01)00884838...
No, this recall is for labeling clarification only. Philips is updating the useful life information for these transducers to help users understand when they should be replaced. There is no safety hazard.
No, you do not need to stop using these probes. This is a labeling update for useful life information, not a safety issue.
Check your V9-2 Transducer Probe for model numbers: 989605466201, 989606717071, 989605492481, 989605456291, or UDI codes starting with (01)00884838...
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2404-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2404-2025 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.
