FDANovember 23, 2022device

Luminos dRF Max (VE10, VF10, VF11)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Under certain unlikely circumstances during a fluoroscopic examination, the imaging system Fluorospot Compact might sporadically display an incorrect air kerma/air kerma rate related to the patient reference point, according to IEC 60601-2-43. There is no impact on workflow or diagnosis. The error can occur only in fluoroscopy systems with a second (overhead) X-ray tube.

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Luminos dRF Max (VE10, VF10, VF11) — Recall Details · AllClear