Philips recalls S5-1 Transducers with serial numbers starting with B1FTT9, B18351, 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 certain S5-1 ultrasound transducers that were refurbished beyond their intended useful life. This means the devices may not function properly or could fail unexpectedly, though the official notice does not specify a risk of injury or damage.
The transducers were refurbished beyond their useful life, meaning they may not perform as intended. This could lead to reduced functionality or failure, but the official notice does not indicate a risk of injury or serious harm.
Users of Philips S5-1 ultrasound transducers with specific serial numbers listed in the recall notice are affected. Medical professionals who use these devices for ultrasound imaging are most at risk.
Check the serial number on your transducer. If it starts with B1FTT9, B18351, B1F61P, or other codes listed in the recall notice, it is affected.
Look for the serial number on your transducer. If it matches the list of affected serial numbers provided in the recall notice, it is part of this recall.
The transducers were refurbished beyond their useful life, which may cause them to malfunction or fail unexpectedly.
The official notice does not specify any remedy or action for affected users.
Check the serial number on your transducer. If it starts with B1FTT9, B18351, B1F61P, or other codes listed in the recall notice, it is affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2058-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2058-2025 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.
