Philips recalls Lumify Diagnostic Ultrasound System models 795005, 795161, 989605449841 for potential imaging failures when used with Apple iOS 18. Affected units may not perform live imaging properly. No remedy specified in recall.
Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
Philips is recalling specific Lumify Diagnostic Ultrasound System models that may not perform live imaging properly when used with Apple iOS 18. This could affect medical imaging accuracy during use. No action is required by the manufacturer as of the recall announcement.
The ultrasound system has compatibility issues with Apple devices running iOS 18, which may cause the system to fail during live imaging. This could lead to inaccurate medical images if the device is used with these specific iOS versions.
Users of the Lumify Diagnostic Ultrasound System with Apple devices running iOS 18 are most at risk. The recall affects specific model numbers listed in the product details.
Check your Lumify Diagnostic Ultrasound System model numbers: 795005, 795161, or 989605449841. Also verify your serial numbers against the list provided in the recall notice.
Review your product's model numbers to see if they match the recalled models: 795005, 795161, or 989605449841.
No action is required by the manufacturer as of the recall announcement. The recall does not specify a remedy.
The recall specifically mentions compatibility issues with Apple devices running iOS 18.
Check your Lumify Diagnostic Ultrasound System model numbers against the list: 795005, 795161, or 989605449841.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0883-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0883-2026 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.
