Philips recalls c5-1 Transducer Probes with specific model numbers for clarification on useful life labeling. 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 c5-1 Transducer Probes to update labeling about their useful life in the field. This is not a safety hazard but a clarification for users to better understand how long these probes should be expected to last.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no actual hazard or risk of injury or damage; this is purely informational to help users understand expected product lifespan.
Users of Philips c5-1 Transducer Probes with the listed model numbers are affected. This recall does not pose a safety risk but aims to clarify product lifespan expectations.
Check your c5-1 Transducer Probe for model numbers listed in the recall (e.g., 989605412042, 989605438541). Also look for the UDI codes provided in the recall list.
Review your c5-1 Transducer Probe's model number to see if it matches any of the listed serial numbers in the recall.
No, this recall is for labeling clarification to define the useful life of the transducers in the field. There is no safety hazard.
No action is required. This is a labeling update to help users understand product lifespan expectations.
Check your probe's model number against the list of model numbers provided in the recall (e.g., 989605412042, 989605438541).
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2352-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2352-2025 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.
