Philips Ultrasound recalls specific C8-4v Transducer Probes with model numbers 989803002685 and others due to labeling clarification for useful life in the field. No safety hazard reported.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound is recalling certain C8-4v Transducer Probes with specific model numbers to clarify labeling for useful life in the field. This recall does not involve a safety hazard but aims to provide better product information.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard described in the recall notice.
Users of Philips Ultrasound C8-4v Transducer Probes with the listed model numbers and UDI codes are affected. Medical professionals using these probes for ultrasound imaging are most at risk.
Check if your probe has model numbers 989803002685, 989605416131, or other listed numbers. Also look for the UDI codes starting with (01)00884838067981(21) followed by specific characters.
Verify your probe's model number and UDI code against the list provided in the recall notice.
No, the recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard reported.
The recall does not require action beyond checking if your product is affected. No repair or replacement is needed.
Check the model number and UDI code on your probe against the list of affected products 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-2358-2025 — Philips Ultrasound Philips Ultrasound Hello, I own a Philips Ultrasound that is covered by recall Z-2358-2025 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.
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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.
