Philips recalls X6-1 transducers refurbished beyond their useful life. Affected models include specific serial numbers and UDI codes. Consumers should check their device details to determine if recalled.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling X6-1 ultrasound transducers that were refurbished beyond their intended useful life. This could lead to potential failure or malfunction if used, though the specific risk isn't detailed in the recall.
The transducers were refurbished beyond their useful life, meaning they may not function properly over time. This could lead to potential failure or malfunction during use, but the recall does not specify a mechanism for injury.
Users of Philips X6-1 ultrasound transducers with the listed serial numbers or UDI codes are affected. Healthcare professionals using these devices for medical imaging are most at risk due to potential failure.
Check for the model numbers 989605409282, 989605438511, or 989605357143, 989605357141. Also look for the UDI codes listed in the recall or the serial numbers provided.
Review the model number and serial number on your Philips X6-1 transducer to see if it matches the listed numbers in the recall.
The transducers were refurbished beyond their useful life, which could lead to potential failure or malfunction.
Check if your model number is 989605409282, 989605438511, 989605357143, or 989605357141, and if your serial number matches the list provided in the recall.
The recall does not specify a need to stop using the transducer; it only indicates potential failure due to refurbishment beyond useful life.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2065-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2065-2025 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.
