Recall Z-1048-2019— LW Scientific, Inc.
Class II · Terminated
Class II FDA medical device recall by LW Scientific, Inc., initiated 2019-02-06, terminated 2021-05-07. FDA's recall record names no specific 510(k) clearance for this event. Product: LW Scientific ZIP IQ PCV Centrifuge, ZIC-24HD-75T3 Rev C Product Usage: used as a general purpose centrifuge to spin down blood in hematocrit tubes. Reason: The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially damaging the surrounding area..
- Recalling firm
- LW Scientific, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-02-06
- Terminated
- 2021-05-07
- Firm location
- Lawrenceville, GA, United States
Product description
LW Scientific ZIP IQ PCV Centrifuge, ZIC-24HD-75T3 Rev C Product Usage: used as a general purpose centrifuge to spin down blood in hematocrit tubes
Reason for recall
The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially damaging the surrounding area.
Data sourced from openFDA. This site is unofficial and independent of the FDA.