Philips recalls BP10-5ec Transducer Probes with specific model numbers for clarification on useful life labeling in medical ultrasound applications.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain BP10-5ec Transducer Probes to clarify their useful life labeling for medical ultrasound use. This recall addresses labeling requirements to ensure proper device management in clinical settings.
The recall focuses on providing clearer labeling for the useful life of ultrasound transducers in the field. This ensures healthcare providers can properly manage device lifespan and avoid potential misuse due to unclear labeling.
Healthcare professionals using Philips BP10-5ec Transducer Probes with the listed model numbers are affected. Patients using these probes for medical ultrasound imaging may be at risk if the labeling is unclear.
Check for model numbers 989605395642 or serial numbers B29VPV, B29VQ6, B2CYJ4, F06M63, F06QYR, B2CY7P, F058R4, B2CY8T, F05YF6, F0628C, B29VPW, F064N9, F078HF, F05Y6Y, B2CYJJ, B2CYD7. These specific identifiers are part of the recalled product.
Verify if your transducer probe has model number 989605395642 or the listed serial numbers.
Philips is recalling these transducers to provide clearer labeling for their useful life in medical ultrasound applications.
Check if your transducer has the listed model numbers or serial numbers. If it does, contact Philips for guidance.
The recall addresses labeling clarity, not a safety hazard. There is no risk of injury reported.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2349-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2349-2025 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.
