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

Genicon Natura Model 210-105-251, 5mm diameter, 150mm length (1 cannula) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope. — recall Z-2277-2020

U.S. FDA — Device Enforcement · United States · 2018-08-21 · Class II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2277-2020
Date of alert
2018-08-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Genicon, Inc.
Product category
device
Product type
Devices
Reported risk: There is potential for the plastic optical tip to become detached from the metal shaft.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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.

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.