Philips recalls X3-1 ultrasound transducers with specific model and serial numbers for labeling clarification on useful life in the field. This update ensures proper product lifecycle management.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain X3-1 ultrasound transducers to clarify their useful life labeling in the field. This recall helps ensure proper product lifecycle management and avoids confusion about when the device should be replaced.
The recall addresses the need for clear labeling of the ultrasound transducer's useful life in the field. This clarification helps prevent confusion about when the device should be replaced, ensuring proper maintenance and safety.
Users of Philips X3-1 ultrasound transducers with the listed model and serial numbers are affected. Healthcare professionals who use these devices for medical imaging are most at risk due to potential labeling confusion.
Check for model numbers 989605440742, 989603002321, 989605388101, 989605440741 or serial numbers ending in 033TVZ, 02Q8R3, 02VLZV, 02WND0, 02ZWBH, 02GP3C, 02YHTG, 02YHPN, 03DTL6, 02JK1H, 02VMJ6, 035Z89, 031C21, 038NQC, 02JL3W, 03C066, 02JK8D.
Verify your X3-1 ultrasound transducer's model number and serial number against the listed numbers to confirm if it is recalled.
Philips is recalling these ultrasound transducers to provide clearer labeling on their useful life in the field, ensuring proper maintenance and replacement.
The recall does not require immediate action; users should check their product details to confirm if it is affected.
No safety risks are associated with this recall. The issue is purely about labeling clarity for useful life management.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1627-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1627-2026 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.
