Class II

Medical Device Recall: CombiDiagnost R90 1.1 (709031)

PHILIPS MEDICAL SYSTEMS · February 11, 2022

Reason for Recall

While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.

Distribution

US Nationwide distribution in the states of CA, FL, GA, IL, IN, KS, MD, ME, MI, MN, NC, NJ, NY, TX, VA, WA.

States Affected

NATIONWIDE

Quantity Affected

130 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1088-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.