Device recall

Z-0772-2019: Leica M220 F12 surgical microscope The Leica M220 F12 surgical microscope is an…

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

Key facts

Recall number (Z-number) Z-0772-2019
Recall event 81903
Product Leica M220 F12 surgical microscope The Leica M220 F12 surgical microscope is an optical instrument for improving the visibility of objects through magnification and illumination. It can be applied for observation and documentation and for human and veterinary medical treatment.
Product code HRM
Recalling firm Leica Microsystems, Inc.
Recall class Class II
Status Terminated
Termination date Apr 2, 2021
FEI number 3000210133

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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)