Device recall

Z-2597-2011: Peloris II Rapid Tissue Processor; Leica Biosystems Melbourne Pty Ltd, Mount…

FDA device recall · Class II · Leica Microsystems, Inc.

Key facts

Recall number (Z-number) Z-2597-2011
Recall event 58502
Product Peloris II Rapid Tissue Processor; Leica Biosystems Melbourne Pty Ltd, Mount Waverly, 3149 VIC, Australia; catalog number 26.0005. This tissue processor prepares tissue samples for sectioning by transforming fixed samples into wax embedded samples. This is achieved by exposing the tissue samples to…
Product code IEO
Recalling firm Leica Microsystems, Inc.
Recall class Class II
Status Terminated
Termination date Jun 20, 2011
FEI number 3000210133

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)