PlainRecalls
FDA Devices Moderate Class II Ongoing

LUMINOS Lotus Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 11574100

Reported: August 14, 2024 Initiated: July 2, 2024 #Z-2527-2024

Product Description

LUMINOS Lotus Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 11574100

Reason for Recall

The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays

Details

Units Affected
26 units
Distribution
US Nationwide distribution.
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
LUMINOS Lotus Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 11574100. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 26 units.
Why was this product recalled?
The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
Which agency issued this recall?
This recall was issued by the FDA Devices on August 14, 2024. Severity: Moderate. Recall number: Z-2527-2024.