Philips recalls L12-3 Transducers with model numbers 989605412072, 989605412071, 989605438571, 989605348241 and UDI codes listed. Devices refurbished beyond useful life pose safety risks.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling L12-3 Transducers that were refurbished beyond their intended useful life. This could lead to safety issues if the device is used after refurbishment.
The transducers were refurbished beyond their useful life, meaning they may not function safely or reliably after refurbishment. This could lead to potential safety issues during medical procedures.
Users of Philips L12-3 Transducers with the listed model numbers and UDI codes are affected. Healthcare professionals using these devices for ultrasound imaging are most at risk.
Check for model numbers 989605412072, 989605412071, 989605438571, or 989605348241. Also look for UDI codes starting with (01)00884838061620(21) followed by specific alphanumeric sequences listed.
Identify if your transducer has model numbers 989605412072, 989605412071, 989605438571, or 989605348241.
Check for UDI codes starting with (01)00884838061620(21) followed by specific alphanumeric sequences listed in the recall.
The transducers were refurbished beyond their useful life, which could lead to safety issues if used after refurbishment.
Check for model numbers 989605412072, 989605412071, 989605438571, or 989605348241, or UDI codes starting with (01)00884838061620(21) followed by specific alphanumeric sequences listed.
The recall does not specify a remedy, so affected users should contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2054-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2054-2025 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.
