RecallRadar

FDA Device recall Z-0772-2019

Leica M220 F12 surgical microscope The Leica M220 F12 surgical microscope is an optical instrument for improving the visibility of objects…

On 2019-01-30 the FDA classified a Class II recall of Leica M220 F12 surgical microscope The Leica M220 F12 surgical microscope is an optical instrument for improving the visibility of objects… by Leica Microsystems, citing the M220 optics may unintentionally drop into the surgical field, risking contact with the patient.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0772-2019
ClassificationClass II
Statusterminated
Initiated2019-01-02
Published2019-01-30
Last updated2026-09-13 11:55 UTC
CompanyLeica Microsystems
DistributionUS

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.

Reason

The M220 optics may unintentionally drop into the surgical field, risking contact with the patient.

Identifiers

code_info
Serial Numbers: 10448367-60618002, 10448367-150317002, 10448367-40518001, 10448367-170417002, 10448367-80517001, 10448…Serial Numbers: 10448367-60618002, 10448367-150317002, 10448367-40518001, 10448367-170417002, 10448367-80517001, 10448367-131117001, 10448367-271117001, 10448367-91017002, 10448367-220318003, 10448367-61017001, 10448367-171117001, 10448367-90418001, 10448367-170417001, 10448367-20418001, 10448367-170718002

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0772-2019%22

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