Philips recalls certain S8-3 Transducer Probes for labeling clarification to define useful life in the field. This recall does not involve safety hazards but aims to improve product labeling.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling specific S8-3 Transducer Probes to clarify their useful life labeling in the field. This recall is about improving product information, not a safety hazard.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard involved.
Users of Philips S8-3 Transducer Probes with the listed model numbers and UDI codes are affected. This recall does not pose a safety risk.
Check if your S8-3 Transducer Probe has model numbers like 989605361882, 989605440752, or UDI codes starting with (01)00884838067806(21).
Identify your S8-3 Transducer Probe model number or UDI code to confirm if it's in the recall list.
No, this recall is for labeling clarification to define the useful life of transducers in the field. There is no safety risk.
No action is required. This recall is about improving labeling information, not a safety issue.
Check the model numbers or UDI codes listed in the recall notice to see if your probe is included.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2397-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2397-2025 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.
