Recall Z-1367-2013— Separation Technology, Inc.
Class II · Terminated
Class II FDA medical device recall by Separation Technology, Inc., initiated 2013-03-13, terminated 2013-12-24. FDA's recall record names no specific 510(k) clearance for this event. Product: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells onto a glass slide from any fluid suspension.. Reason: Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges manufactured prior to January 1, 2013 for having the potential to start up unexpectedly when encountering an electrostatic discharge..
- Recalling firm
- Separation Technology, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-03-13
- Terminated
- 2013-12-24
- Firm location
- Sanford, FL, United States
Product description
SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells onto a glass slide from any fluid suspension.
Reason for recall
Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges manufactured prior to January 1, 2013 for having the potential to start up unexpectedly when encountering an electrostatic discharge.
Data sourced from openFDA. This site is unofficial and independent of the FDA.