Philips recalls L8-4 transducers refurbished beyond their useful life. These devices may not function safely. Affected units have specific model and serial numbers.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling L8-4 ultrasound transducers that were refurbished beyond their intended useful life. This means the devices may not function safely, potentially causing harm if used.
The transducers were refurbished beyond their useful life, meaning they may not function safely. This could lead to improper imaging results or device failure during use.
Users of Philips L8-4 transducers with specific model and serial numbers are affected. Healthcare professionals using these devices for medical imaging are most at risk.
Check for model numbers 989605440811 or 989605440812 on the transducer. Look for serial numbers like B0LZNN, 03BPVM, or 02KMFZ on the device.
Identify the model number (989605440811 or 989605440812) and serial number (e.g., B0LZNN) on the transducer.
The transducers were refurbished beyond their useful life, which may cause them to malfunction or fail during use.
Check for model numbers 989605440811 or 989605440812 and serial numbers like B0LZNN, 03BPVM, or 02KMFZ.
The recall record does not specify a remedy, so contact Philips for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2056-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2056-2025 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.
