Philips recalls S7-3t Transducers with model numbers 989605440772, 989605440771, 989605439232, 989605406772, 989605439231, 989606708921, 989803002661 and UDI codes listed. Devices refurbished beyond useful life.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling S7-3t Transducers that were refurbished beyond their useful life. This means the devices may not function properly and could pose a risk of malfunction. Affected units have specific model numbers and UDI codes listed in the recall notice.
The transducers were refurbished beyond their intended useful life, which can lead to potential malfunction. This may result in improper imaging or device failure, but does not typically cause injury or serious harm under normal use conditions.
Users of Philips S7-3t Transducers with the listed model numbers and UDI codes are affected. Healthcare professionals and medical staff who use these devices for ultrasound imaging are most at risk.
Check if your Philips S7-3t Transducer has model numbers 989605440772, 989605440771, 989605439232, 989605406772, 989605439231, 989606708921, or 989803002661. Also, look for the UDI codes listed in the recall notice.
Verify if your Philips S7-3t Transducer has the listed model numbers or UDI codes from the recall notice.
Philips recalls these transducers because they were refurbished beyond their useful life, which may lead to potential malfunction.
No action is needed if your transducer is not listed in the recall notice.
The recall states the transducers were refurbished beyond useful life, but does not indicate a risk of injury or serious harm under normal use conditions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2060-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2060-2025 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.
