Recall Z-3175-2018— Leica Microsystems, Inc.
Class II · Terminated
Class II FDA medical device recall by Leica Microsystems, Inc., initiated 2018-09-04, terminated 2021-08-17. FDA's recall record names no specific 510(k) clearance for this event. Product: Leica M525 F20 Surgical Microscope System. Reason: The firm received complaints that the instrument tipped over when the swing arm was fully extended..
- Recalling firm
- Leica Microsystems, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-09-04
- Terminated
- 2021-08-17
- Firm location
- Buffalo Grove, IL, United States
Product description
Leica M525 F20 Surgical Microscope System
Reason for recall
The firm received complaints that the instrument tipped over when the swing arm was fully extended.
Data sourced from openFDA. This site is unofficial and independent of the FDA.