Philips recalls C5-2 Transducers with model numbers 989605389242 and others due to being refurbished beyond useful life. Consumers should stop using affected units.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling C5-2 Transducers that were refurbished beyond their useful life. This could lead to potential failure or malfunction. Affected units should be stopped using immediately.
The transducers were refurbished beyond their intended useful life, meaning they may not function properly and could fail or malfunction during use. This poses a risk of potential failure or malfunction in medical settings.
Users of Philips C5-2 Transducers with specific model numbers listed in the recall are affected. Healthcare professionals using these devices for ultrasound imaging are most at risk.
Check for model numbers 989605389242, 989605454101, 989605398211, and others listed in the recall. Also look for unique identifiers (UDI) starting with (01)00884838067424(21) followed by specific codes.
Immediately stop using the affected Philips C5-2 Transducer if it matches the model numbers or unique identifiers listed in the recall.
Affected model numbers include 989605389242, 989605454101, 989605398211, and others listed in the recall.
Check the model number on the transducer or look for the unique identifier (UDI) starting with (01)00884838067424(21) followed by specific codes listed in the recall.
Immediately stop using the transducer and 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-2050-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2050-2025 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.
