Philips recalls D2cwc Transducer Probes with specific model numbers for labeling clarification on useful life in the field. No immediate safety risk but requires updated labeling.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain D2cwc Transducer Probes to clarify their useful life in the field through labeling. This is a labeling update, not a safety hazard. The product remains safe to use but needs updated labeling information.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard; this is a labeling update to help users understand the product's expected lifespan.
Users of Philips D2cwc Transducer Probes with the listed model numbers are affected. This recall is for labeling clarification, not a safety issue.
Check your D2cwc Transducer Probe for model numbers 989605438551, 989605412052, 989605400802 or UDI codes listed in the recall notice. The recall covers specific model variants.
Identify your D2cwc Transducer Probe's model number from 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, the product remains safe to use. This is a labeling update for clarity on the product's expected lifespan.
Check your model number against the list of affected models or UDI codes provided in the recall notice.
We’ve drafted a message you can send Philips Ultrasound to request your refund or repair — edit it as you like.
Subject: Recall Z-2366-2025 — Philips Ultrasound Philips Ultrasound Hello, I own a Philips Ultrasound that is covered by recall Z-2366-2025 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.
