Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,

Recall Insight

This FDA Devices action (record #Z-0883-2026) was formally reported on December 10, 2025, with the manufacturer initiating the action on October 31, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Philips Ultrasound, LLC is listed as the recalling firm, operating out of Bothell, WA. Federal records indicate 4,819 systems units are affected.

The documented reason for this recall is: Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining. Distribution data in the federal record shows the product reached: Worldwide US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, S…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 1 year old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.