Philips recalls mC12-3 Transducer Probes with specific UDI codes for labeling clarification on useful life in the field. No immediate safety risk but requires label updates.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain mC12-3 Transducer Probes to clarify their useful life in the field through labeling. This is a labeling update to help users understand how long the transducer should be expected to function before needing replacement. There is no safety risk involved.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. This is not a safety hazard but a labeling update to help users understand when transducers should be replaced based on their expected lifespan.
Users of Philips mC12-3 Transducer Probes with the specific UDI codes listed in the recall notice are affected. The recall targets medical ultrasound equipment users.
Check your mC12-3 Transducer Probe for the UDI codes listed in the recall notice. These codes follow the format (01)00884838093935(21) followed by a series of characters.
Look for the UDI codes on your mC12-3 Transducer Probe to see if they match the list provided in the recall notice.
No, this recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety risk involved.
No action is required. This is a labeling update to help users understand when transducers should be replaced based on their expected lifespan.
Check for UDI codes following the format (01)00884838093935(21) followed by a series of characters as listed in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2383-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2383-2025 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.
