Becton Dickinson & Company: Medical Device Recall in 2022 - (Recall #: Z-0665-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class III

Date Initiated: January 6, 2022

Date Posted: March 2, 2022

Recall Number: Z-0665-2022

Event ID: 89486

Reason for Recall:

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

Status: Ongoing

Product Quantity: 288,152,790 Units

Code Information:

All Lots within Expiry Catalog No: 364902 UDI: (01)50382903649025 Catalog Number: 36490200 UDI:(01)60382903649022

Distribution Pattern:

US Nationwide distribution in the state of IL.

Voluntary or Mandated:

Voluntary: Firm initiated