Philips recalls L9-3 Transducers with model numbers 989605353301, 989605353303, 989605387361. These devices were refurbished beyond their useful life, posing a risk of failure.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling L9-3 Transducers that were refurbished beyond their useful life. This could lead to device failure, though the specific risk isn't detailed in the recall.
The transducers were refurbished beyond their intended useful life, which could cause them to fail. This failure might lead to improper medical imaging or device malfunction, though the exact risk isn't specified.
Users of Philips L9-3 Transducers with model numbers 989605353301, 989605353303, or 989605387361 are affected. Healthcare professionals using these transducers for medical imaging are most at risk.
Check for model numbers 989605353301, 989605353303, or 989605387361 on the transducer. Serial numbers starting with B0ZTD1, 03F40C, or similar patterns also indicate affected units.
Look for model numbers 989605353301, 989605353303, or 989605387361 on the transducer.
Reach out to Philips customer support for further assistance with the recall.
The transducers were refurbished beyond their useful life, which could cause failure.
Check the model number and contact Philips customer support for guidance.
The recall states the transducers were refurbished beyond their useful life, but specific safety risks aren't detailed.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2057-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2057-2025 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.
