FDASeptember 24, 2015device

MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.

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

The hazard

Display freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user.

What to do

FDA enforcement status: Terminated

Brands named

siemens medical solutionssiemenssiemens medical

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →