Philips recalls specific C5-2 Transducer Probe models due to labeling for useful life clarification. No safety hazard exists; this is a labeling update to help users understand product lifespan.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain C5-2 Transducer Probes to clarify their useful life in the field through updated labeling. This is not a safety hazard but a labeling update to help users understand how long the product should be expected to function.
This recall is for labeling clarification to define the useful life of the transducers in the field. There is no safety hazard or risk of injury; it is a labeling update to help users understand the product's expected lifespan.
Users of Philips C5-2 Transducer Probes with the listed model numbers and UDI codes are affected. Healthcare professionals using these probes for ultrasound imaging are most at risk.
Check your C5-2 Transducer Probe for model numbers listed in the recall (e.g., 989605358813) or Unique Device Identifiers (UDIs) like (01)00884838067424(21)B200XV.
Look for model numbers or UDI codes on your C5-2 Transducer Probe to see if they match the recalled list.
No, this recall is for labeling clarification to define the useful life of the transducers in the field. There is no safety hazard.
No, this is a labeling update to help users understand the product's expected lifespan. You do not need to stop using them.
Check the model number or Unique Device Identifier (UDI) on your transducer against the list provided 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-2353-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2353-2025 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.
