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

Recall Z-1998-2014 — 07-150-07 MIZUHO, MAL DISP DOPPLER PROBE BX 4, REF 138200 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.

U.S. FDA — Device Enforcement · United States · 2014-05-28 · 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-1998-2014
Date of alert
2014-05-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Vascular Technology, Inc.
Product category
device
Product type
Devices
Reported risk: Report of the product penetrating the sterile barrier; this could render the product unsterile.
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.