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Becton Dickinson & Company recalls BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a ca
Recalled March 2, 2022 · FDA recall Z-0665-2022 · Becton Dickinson &
Hazard
May shed contaminant particles into the urine specimen that may be misidentified as Red Blood Cells when used in conjunction with the Sysmex UF-1000i or UX-2000 Analyzers and lead to false elevations in RBC counts · FDA Class III
Units
288,152,790 Units
Sold at
US Nationwide distribution in the state of IL.
Description
May shed contaminant particles into the urine specimen that may be misidentified as Red Blood Cells when used in conjunction with the Sysmex UF-1000i or UX-2000 Analyzers and lead to false elevations in RBC counts
Product
BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port equipped with a threaded female luer during blood or urine sample collection using evacuated BD Vacutainer Blood or Urine Collection Tubes Catalog Number: 364902, 36490200
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →