Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Leica Microsystems M220 F12 Microscope Systems Recalled by Leica Microsystems, Inc. Due to In May 2021, Leica Microsystems received one (1)...
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 Microsystems M220 F12 Microscope Systems
Quantity: 2,800
Why Was This Recalled?
In May 2021, Leica Microsystems received one (1) complaint pertaining to the M220 F12 Surgical Microscope system. There was no patient injury reported for this complaint. However, the identified defect carries some potential injury risk. In the event that this defect may occur, the M220 optics carrier may unintentionally drop into the surgical field, risking contact with the patient.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Leica Microsystems, Inc.
Leica Microsystems, Inc. has 40 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report