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Philips Medical Systems Nederland B.V. recalls Allura Xper series
Recalled September 13, 2023 · FDA recall Z-2402-2023 · Philips Medical Systems Nederland B.V
Hazard
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation · FDA Class II
Units
5432 systems in total
Sold at
US Nationwide Distribution
Description
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
Product
Allura Xper series
Manufacturer(s)
Philips Medical Systems Nederland B.V.
Made in
Netherlands
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →