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Philips North America Llc recalls CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system
Recalled November 15, 2023 · FDA recall Z-0271-2024 · Philips North America
Hazard
Potential for units suspended on the ceiling to fail and fall. · FDA Class II
Units
46 units
Sold at
Nationwide distribution.
Description
Potential for units suspended on the ceiling to fail and fall.
Product
CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →