Recall Z-2660-2017— Leica Microsystems, Inc.
Class II · Ongoing
Class II FDA medical device recall by Leica Microsystems, Inc., initiated 2017-06-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Nussloch GmbH ASP6025 Tissue Processor. Reason: Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit..
- Recalling firm
- Leica Microsystems, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2017-06-19
- Firm location
- Buffalo Grove, IL, United States
Product description
Nussloch GmbH ASP6025 Tissue Processor
Reason for recall
Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit.
Data sourced from openFDA. This site is unofficial and independent of the FDA.