Philips recalls C10-4ec Transducer Probes with specific model numbers for clarification on useful life labeling in medical ultrasound applications.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain C10-4ec Transducer Probes to clarify labeling for the useful life of ultrasound transducers in the field. This is a labeling update, not a safety hazard.
The recall involves updating labeling to define the useful life of ultrasound transducers in the field. This is a clarification of labeling, not a safety hazard.
Medical professionals using Philips C10-4ec Transducer Probes with the listed model numbers are affected. The risk is minimal as this is a labeling clarification for useful life.
Check for model numbers 989605413712, 989605438601, 989605391092, or the UDI codes listed in the recall notice. The product is a medical ultrasound transducer probe.
Look for the model numbers or UDI codes listed in the recall notice to confirm if your transducer probe is affected.
No, this recall is for clarification on useful life labeling, not a safety hazard.
No, this is a labeling update for useful life information; no action is required beyond checking the model numbers.
No action is required as this is a labeling clarification, not a safety issue.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2351-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2351-2025 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.
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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.
