Philips recalls X8-2t Transducers with serial numbers starting with B2JH... due to being refurbished beyond useful life. No safety risk described in official notice.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling X8-2t Transducers that were refurbished beyond their useful life. This means the devices may not function properly and could pose a risk of malfunction. Consumers should check if their device has the listed serial numbers and take appropriate action.
The transducers were refurbished beyond their useful life, meaning they may not function properly and could malfunction. However, the official recall notice does not describe any specific hazard mechanism or risk of injury.
Users of Philips X8-2t Transducers with the specific serial numbers listed in the recall notice are affected. Medical professionals using these devices for ultrasound imaging are most at risk.
Check if your Philips X8-2t Transducer has a serial number starting with B2JH followed by the listed codes (e.g., B2JH74, B29746, etc.). The full list of affected serial numbers is provided in the recall notice.
Look for the serial number on your Philips X8-2t Transducer. If it starts with B2JH followed by the listed codes (e.g., B2JH74, B29746), it is affected.
The recall notice states the transducers were refurbished beyond their useful life, but does not describe any specific hazard or risk of injury.
The recall notice does not specify a remedy or action for affected devices. Consumers should check with Philips for further instructions.
The official recall notice does not describe any specific hazard mechanism or risk of injury.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2067-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2067-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
