Philips recalls eL18-4 EMT Transducers refurbished beyond useful life. Affected units may have reduced safety. Contact Philips for details.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling eL:18-4 EMT Transducers that were refurbished beyond their intended useful life. This could lead to reduced safety and potential failure.
Refurbished transducers may not function safely after their intended useful life. This could lead to reduced performance or failure during medical procedures.
Users of Philips eL18-4 EMT Transducers that were refurbished beyond their useful life. Medical professionals using these transducers are most at risk.
Check for model number 989605431531 or serial number B29W3Y on the transducer. These units were sold with the UDI (01)00884838070806(21)B29W3Y.
Look for model number 989605431531 or serial number B29W3Y on the transducer.
The transducers were refurbished beyond their useful life, which could lead to reduced safety and potential failure.
Check for model number 989605431531 or serial number B29W3Y on the transducer.
The recall does not specify a remedy, so contact Philips directly for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2053-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2053-2025 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.
