FDAFDA · Food and drugs·Recall number 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 hematocrit tubes
Published April 3, 2019 · Recall initiated: February 6, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- LW Scientific, Inc.
- Distributor
- Worldwide Distribution - US Nationwide and the countries of Philippines, Honduras, El Salvador, Australia, Guatemala, Canada, Singapore, Australia, Peru, Nicaragua, Trinidad and Tobago, and New Zealand
- Lot
- 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, 24H1804258, 24H1804259, 24H1804260, 24H1804261, 24H1804262, 24H1804263, 24H1804264, 24H1804265, 24H1804266, 24H1804267, 24H1804268, 24H1804269, 24H1804270, 24H1804271, 24H1804272, 24H1804273, 24H1804274, 24H1804278, 24H1804279, 24H1804280, 24H1804281, 24H1804282, 24H1810336, 24H1810337, 24H1810338, 24H1810339, 24H1810340, 24H1810341, 24H1810342, 24H1810343, 24H1810352, 24H1810353, 24H1810355, 24H1810360, 24H1810361, 24H1810362, 24H1810363, 24H1810367, 24H1810368, 24H1810369, 24H1810370, 24H1810371, 24H1810373, 24H1810386, 24H1810387, 24H1810393, 24H1810394, 24H1810395, 24H1810405, 24H1810410, 24H1810412, 24H1810413, 24H1810414, 24H1810415, 24H1810416, 24H1810417, 24H1810418, 24H1810419, 24H1810424, 24H1810425, 24H1810428
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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