Becton Dickinson & Co.: Medical Device Recall in 2023 - (Recall #: Z-0110-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023

Product Classification:

Class II

Date Initiated: September 12, 2023

Date Posted: October 18, 2023

Recall Number: Z-0110-2024

Event ID: 93097

Reason for Recall:

Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling issue where duplicate barcode sequence numbers have been identified on more than one vial.

Status: Ongoing

Product Quantity: 781,600 vials

Code Information:

UDI-DI: 038290HXRPGWNNMN; Lot Numbers: 3062843 3062846 3062849 3062847 3067489 3067488

Distribution Pattern:

Worldwide - US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated