Philips recalls X5-1 Transducer Probes with specific model numbers for clarification on useful life labeling in the field. No safety hazard exists; this is a labeling update to help users understand product lifespan.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling X5-1 Transducer Probes with specific model numbers to provide clearer labeling about their useful life in the field. This is not a safety hazard but a labeling update to help users understand how long the probes should be expected to function before replacement.
This recall is for labeling clarification only. The product itself does not have a safety hazard; Philips is updating the labeling to help users understand the expected useful life of the transducers in the field.
Users of Philips X5-1 Transducer Probes with the listed model numbers may need to check their product's useful life. This recall does not involve safety risks but is a labeling update.
Check your X5-1 Transducer Probe for model numbers listed in the recall (e.g., 989605400802, 989605438491). Also look for the UDI codes provided in the recall list.
Identify your X5-1 Transducer Probe's model number and UDI code to see if it's in the recall list.
No, this recall is for labeling clarification only. There is no safety hazard involved.
No, this recall does not require stopping use. It's a labeling update to help users understand the product's useful life.
Check your model number and UDI code against the list provided in the recall.
We’ve drafted a message you can send Philips Ultrasound to request your refund or repair — edit it as you like.
Subject: Recall Z-2408-2025 — Philips Ultrasound Philips Ultrasound Hello, I own a Philips Ultrasound that is covered by recall Z-2408-2025 from Philips Ultrasound. 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.
