Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0265-2016 — MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.

U.S. FDA — Device Enforcement · United States · 2015-09-24 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0265-2016
Date of alert
2015-09-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc
Product category
device
Product type
Devices
Reported risk: Display freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.