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

Recall Z-2177-2013 — Surgical microscope The device is used to improve the visibility of objects through magnification and illumination and can be applied for observation and documentation and for human veterinary medical treatment.

U.S. FDA — Device Enforcement · Switzerland · 2012-12-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2177-2013
Date of alert
2012-12-18
Country / jurisdiction
Switzerland
Risk level
Class II
Risk type
recall
Brand
Leica Microsystems (Schweiz) Ag
Product category
device
Product type
Devices
Reported risk: The brake in the Z axis and/or brakes in the AB and C axes failed during installation.
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.

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