Philips recalls mC7-2 Transducer Probes with specific UDI codes for labeling clarification on useful life in field use. No safety hazard exists; this is a labeling update for better product management.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain mC7-2 Transducer Probes to update labeling about their useful life in field use. This is not a safety hazard but a labeling clarification for better product management.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard or risk of injury.
Users of Philips mC7-2 Transducer Probes with the listed UDI codes are affected. This recall does not pose a safety risk.
Check your mC7-2 Transducer Probe for the UDI codes listed in the recall notice. These codes are unique identifiers for the affected units.
Look for the UDI codes listed in the recall notice on your transducer probe.
No, this recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard.
No, this recall does not require stopping use. It is a labeling update for better product management.
No action is needed. This recall is for labeling clarification, not a safety issue.
We’ve drafted a message you can send Philips Ultrasound to request your refund or repair — edit it as you like.
Subject: Recall Z-2384-2025 — Philips Ultrasound Philips Ultrasound Hello, I own a Philips Ultrasound that is covered by recall Z-2384-2025 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.
