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Becton Dickinson & Company recalls BD Microtainer PSTTubes with LH (Lithium Heparin) Part/Catalog Number:365985
Recalled October 16, 2019 · FDA recall Z-0059-2020 · Becton Dickinson &
Hazard
Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results. · FDA Class II
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Description
Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
Product
BD Microtainer PSTTubes with LH (Lithium Heparin) Part/Catalog Number:365985
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →