Philips recalls V6-2 Transducers (model numbers 989605357563, 989605415042, etc.) due to being refurbished beyond useful life. No remedy specified in official notice.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling V6-2 Transducers that were refurbished beyond their intended useful life. This could lead to reduced performance or failure, but the official notice does not specify a risk of injury or damage.
The transducers were refurbished beyond their useful life, meaning they may not function properly or could fail prematurely. This could lead to inaccurate imaging or device failure during use, but the official notice does not indicate a risk of injury.
Users of Philips V6-2 Transducers with the listed model numbers and serial codes are affected. Most at risk are medical professionals who use these devices for ultrasound imaging.
Check for model numbers 989605357563, 989605415042, 989605437982, 989605387201, 989605357561, or serial numbers listed in the UDI codes. These transducers were sold by Philips Ultrasound, Inc.
Identify if your transducer has model numbers 989605357563, 989605415042, 989605437982, 989605387201, or 989605357561.
Check if your transducer's serial number matches any listed in the UDI codes provided in the recall notice.
The official recall notice states the transducers were refurbished beyond useful life, but does not mention any risk of injury or serious harm.
No, the recall does not require stopping use. The official notice does not specify a remedy or action to take.
Check for model numbers 989605357563, 989605415042, 989605437982, 989605387201, 989605357561, or serial numbers listed in the UDI codes provided in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2062-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2062-2025 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.
