Philips recalls X7-2 Ultrasound Transducers with specific model numbers for clarification on useful life in field use. No immediate safety risk but requires labeling updates.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain X7-2 ultrasound transducers to clarify their useful life in field use. This recall does not involve safety risks but ensures proper labeling for product longevity.
The recall addresses the need for clearer labeling to define how long these ultrasound transducers can be safely used in medical settings. This helps ensure proper maintenance and replacement timelines without causing safety issues.
Healthcare professionals using Philips X7-2 ultrasound transducers with the listed model numbers are affected. Those who use these devices for medical imaging are most at risk of confusion about product lifespan.
Check for model numbers 989605388121, 989605347571, or 989605347573 on the transducer. Serial numbers like 03FG1T, 031LM2, 032Q7G, 0344RZ, or 033VM9 also indicate the recalled units.
Check the transducer for model numbers 989605388121, 989605347571, or 989605347573 and serial numbers like 03FG1T, 031LM2, 032Q7G, 0344RZ, or 033VM9.
Philips is recalling these ultrasound transducers to clarify their useful life in field use, ensuring proper labeling for product longevity without safety risks.
No, this recall is for labeling clarification only and does not involve safety hazards.
Check the model and serial numbers listed in the recall notice to confirm if your transducer is affected. No action is needed beyond verifying the product details.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1628-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1628-2026 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.
