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

Recall Z-0799-2014 — Compensator Slider Lambda 6x20 component (part number 473704-0000-000) utilized on all upright ZEISS microscopes (Axio Imager, Axio Scope. A1, Axio Lab. A1). Component used to determine composition of urinary calculi, urinary sediments, bio-crystallates and diagnosis of pathological characteristi

U.S. FDA — Device Enforcement · United States · 2013-12-20 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0799-2014
Date of alert: 2013-12-20
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zeiss, Carl Inc
Product category: device
Product type: Devices

Reported risk: Carl Zeiss Microscopy, LLC has recalled the Compensator Slider Lamda 6x20 component utilized on Standard Pathology Microscopes due to misalignment of the lambda plate.

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.

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.

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