FDA Device recall Z-1048-2019
LW Scientific ZIP IQ PCV Centrifuge, ZIC-24HD-75T3 Rev C Product Usage: used as a general purpose centrifuge to spin down blood in hematocr…
- FDA Device
- Class II
- terminated
- Published 2019-04-03
On 2019-04-03 the FDA classified a Class II recall of LW Scientific ZIP IQ PCV Centrifuge, ZIC-24HD-75T3 Rev C Product Usage: used as a general purpose centrifuge to spin down blood in hematocr… by Lw Scientific, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1048-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-02-06 |
| Published | 2019-04-03 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Lw Scientific |
| Distribution | US |
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.
Identifiers
| code_info | Serial Numbers: 24H1712209, 24H1712302, 24H1712305, 24H1712306, 24H1712308, 24H1712313, 24H1712314, 24H1712315, 24H171…Serial Numbers: 24H1712209, 24H1712302, 24H1712305, 24H1712306, 24H1712308, 24H1712313, 24H1712314, 24H1712315, 24H1712316, 24H1712319-1, 24H1804183, 24H1804184, 24H1804185, 24H1804186, 24H1804187, 24H1804188, 24H1804189, 24H1804190, 24H1804191, 24H1804192, 24H1804193, 24H1804194, 24H1804195, 24H1804196, 24H1804197, 24H1804198, 24H1804199, 24H1804200, 24H1804201, 24H1804202, 24H1804207, 24H1804208, 24H1804209, 24H1804210, 24H1804211, 24H1804212, 24H1804213, 24H1804214, 24H1804215, 24H1804216, 24H1804217, 24H1804218, 24H1804219, 24H1804220, 24H1804221, 24H1804222, 24H1804223, 24H1804224, 24H1804225, 24H1804226, 24H1804227, 24H1804228, 24H1804229, 24H1804230, 24H1804231, 24H1804232, 24H1804233, 24H1804234, 24H1804235, 24H1804236, 24H1804237, 24H1804238, 24H1804239, 24H1804240, 24H1804241, 24H1804242, 24H1804243, 24H1804244, 24H1804245, 24H1804246, 24H1804247, 24H1804248, 24H1804249, 24H1804250, 24H1804251, 24H1804252, 24H1804253, 24H1804254, 24H1804255, 24H1804256, 24H1804257, 24H180425 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1048-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.