Becton Dickinson & Co.: Medical Device Recall in 2022 - (Recall #: Z-0630-2022)

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 Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings. Catalog Number: 256066

Product Classification:

Class II

Date Initiated: January 5, 2022

Date Posted: February 16, 2022

Recall Number: Z-0630-2022

Event ID: 89358

Reason for Recall:

May have the potential to overheat and/or cause fire, the issue can occur when an unauthorized alternative AC power adapter, and not the one provided by BD is used to power the instrument.

Status: Ongoing

Product Quantity: 126,952 Analyzers Updated:129, 848 Analyzers

Code Information:

All unexpired analyzers (Exp. Date 12/2021 - 8/2024) UDI: 00382902560661

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Armenia, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Dominican Republic, Ecuador, Fiji, Guatemala, Hong Kong, Honduras, Haiti, Indonesia, India, Jamaica, Cambodia, South Korea, Macao, Mexico, New Zealand, Panama, Peru, Philippines, Singapore, El Salvador, Thailand, Trinidad and Tobago, Taiwan, Uruguay, Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated