Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Leica ARveo and M530 OH6 microscope systems. Recalled by Leica Microsystems, Inc. Due to Possible unintended interruption of surgical procedures due to...

Date: May 20, 2020
Company: Leica Microsystems, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Leica Microsystems, Inc. directly.

Affected Products

Leica ARveo and M530 OH6 microscope systems.

Quantity: Domestic distribution 65 devices. International distribution 12 devices. Total of devices distributed 77.

Why Was This Recalled?

Possible unintended interruption of surgical procedures due to equipment shutdown, related to changes in voltage.

Where Was This Sold?

This product was distributed to 25 states: AL, AZ, AR, CA, CT, DE, FL, IL, KY, LA, MI, MN, MO, NY, NC, OH, OR, TN, TX, UT, VA, WA, WV, WI, DC

Affected (25 states)Not affected

About Leica Microsystems, Inc.

Leica Microsystems, Inc. has 40 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report