Philips recalls L15-7IO Transducer Probes for labeling clarity on useful life in field use. No immediate safety risk but requires updated labeling for proper maintenance.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling L15-7:7IO transducer probes to clarify their useful life in field use. This is a labeling update to help users understand maintenance requirements, not a safety hazard.
The recall is for labeling clarification to define the useful life of transducers in field use. This ensures proper maintenance and usage guidance without posing a safety risk.
Users of Philips L15-7IO transducer probes for medical ultrasound imaging. Healthcare professionals and medical facilities using these probes are most affected.
Check for the L15-7IO model transducer probe. The product has no specific model number or serial number listed in the recall notice.
Check the transducer probe for updated labeling on useful life in field use.
No, this recall is for labeling clarification to define the useful life of transducers in field use, not a safety hazard.
No, the recall does not require stopping use; it's for labeling updates to help with maintenance.
The recall does not specify any action for disposal or return; it's a labeling update.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2378-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2378-2025 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.
