Diagnostic Ultrasound System Correction: Philips Ultrasound Issues Updated Use Instructions For Lumify Diagnostic Ultrasound System
Recall Summary Philips is correcting instructions for its Lumify Diagnostic Ultrasound System due to a software or transducer connection issue that may cause the device to lose scanning capability or experience scanning delays. The problem affects users of the Lumify Diagnostic Ultrasound System. Philips has issued updated use instructions to address this issue.
- Product
- Lumify Diagnostic Ultrasound System
- Reason
- A software app or transducer connection problem with the Philips Lumify diagnostic ultrasound system can result in loss of or delays in scanning functionality.
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-MEDWATCH-RSS
- Recall date
- 2026-10-19
- Status
- Ongoing
Official recall notice from FDA-MEDWATCH-RSS
Recall details on Nibble Recalls: https://trynibble.app/recalls/ac14b084-2048-448e-90f0-4da7b81be50f