Recall Z-2659-2018— Leica Microsystems, Inc.
Class II · Terminated
Class II FDA medical device recall by Leica Microsystems, Inc., initiated 2018-06-25, terminated 2019-02-26. FDA's recall record names no specific 510(k) clearance for this event. Product: Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.. Reason: Recall is due to a design weakness of the power insert module..
- Recalling firm
- Leica Microsystems, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-06-25
- Terminated
- 2019-02-26
- Firm location
- Buffalo Grove, IL, United States
Product description
Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.
Reason for recall
Recall is due to a design weakness of the power insert module.
Data sourced from openFDA. This site is unofficial and independent of the FDA.