Becton Dickinson & Company: Medical Device Recall in 2022 - (Recall #: Z-0095-2023)

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 Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting, separating, and processing blood for blood alcohol determination.

Product Classification:

Class II

Date Initiated: September 15, 2022

Date Posted: October 26, 2022

Recall Number: Z-0095-2023

Event ID: 90824

Reason for Recall:

The affected product contains isobutylene which has recently demonstrated potential interference in determination of methanol by gas chromatography methods. The interference may lead to false positive results in methanol testing.

Status: Ongoing

Product Quantity: 2,196,000

Code Information:

UDI-DI: Case: 50382903670012; Shelf: 30382903670018; Each: 00382903670017; ALL LOTS are affected.

Distribution Pattern:

Distribution US nationwide, Canada, New Zealand, and Hong Kong.

Voluntary or Mandated:

Voluntary: Firm initiated