Philips recalls specific L12-5 50 Transducer Probe models with UDI codes for labeling clarification on useful life in the field. No safety risk reported.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain L12-5 50 Transducer Probes to clarify their useful life in the field through labeling. This is a labeling update, 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 described.
Users of Philips L12-5 50 Transducer Probes with the listed model numbers or UDI codes are affected. This recall involves labeling clarification, not safety risks.
Check if your L12-5 50 Transducer Probe has a model number from the list or a UDI code starting with (01)00884838067851(21) followed by specific characters.
Review your product's model number against the provided list of model numbers or UDI codes to confirm if it's affected.
No, this recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety risk reported.
No action is required. This is a labeling update, not a safety hazard.
Check your product's model number against the list of model numbers or UDI codes provided in the recall notice.
We’ve drafted a message you can send Philips Ultrasound to request your refund or repair — edit it as you like.
Subject: Recall Z-2376-2025 — Philips Ultrasound Philips Ultrasound Hello, I own a Philips Ultrasound that is covered by recall Z-2376-2025 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.
