ClearanceBrief
Recall Z-2309-2019 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

Becton Dickinson & Company

BD Vacutainer LH (Lithium Heparin) 68 I.U. Plus Blood Collection Tubes, Catalog Number 368884

DateJun 12, 2019
StatusTerminated
ReasonFalse elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
Root causeDevice Design
ActionUrgent Medical Device Correction notification letters dated 6/12/19 were sent to customers.
Quantity1,436,228,004 total
DistributionWorldwide Distribution, including US Nationwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K901449VACUTAINER PLUS WITH HEMOGARD CLOSURE
Bd Becton Dickinson Vacutainer Systems Preanalytic, Aug 9, 1990