Philips recalls S7-2 Transducers with model numbers 989605440772, 989605440771, 989803002261 due to being refurbished beyond useful life. No remedy specified in recall notice.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling certain S7-2 Transducers that were refurbished beyond their intended useful life. This means the devices may not function properly and could pose risks if used.
The transducers were refurbished beyond their useful life, meaning they may not function properly and could lead to inaccurate imaging results or device failure.
Users of Philips S7-2 Transducers with model numbers 989605440772, 989605440771, or 989803002261 are affected. Medical professionals using these devices for ultrasound imaging are most at risk.
Check for model numbers 989605440772, 989605440771, or 989803002261 on the transducer. Also look for serial numbers listed in the UDI codes provided in the recall notice.
Identify if your transducer has model numbers 989605440772, 989605440771, or 989803002261.
The transducers were refurbished beyond their useful life, which may cause them to malfunction.
The recall notice does not specify a remedy, so you should check with Philips for further instructions.
The recall indicates potential malfunction due to being refurbished beyond useful life, but no specific safety hazards are described.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2059-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2059-2025 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.
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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.
