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

Recall Z-1446-2013 — LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848; 14060546846; 14060546845; 14060546933; 14060546932; 14060546852; 14060546850; 14060546847. The intended use of this device is for storage of specimens/tissues during processing.

U.S. FDA — Device Enforcement · United States · 2013-04-04 · 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-1446-2013
Date of alert
2013-04-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Leica Microsystems, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
14060546848
Reported risk: An LPC Fine Mesh Cassette failed to stay closed during processing operations.
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.