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Becton Dickinson & Company recalls BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 3650
Recalled April 4, 2018 · FDA recall Z-1180-2018 · Becton Dickinson &
Hazard
Increased amount of residual blood present on the top of stopper well after venipuncture · FDA Class II
Units
1,976,000 tubes
Sold at
USA (nationwide)
Description
Increased amount of residual blood present on the top of stopper well after venipuncture
Product
BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 365043, 365044, 365045 & 365047 Used to collect, separate, process, transport and store venous blood samples for use in chemistry determinations, therapeutic drug monitoring and zinc testing in plasma for in vitro diagnostic use.
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →