Reported May 22, 2019 · Terminated

BD Veritor System Reader -In Vitro Diagnostic for use with BD Veritor System Test Kit Devices Catalog Number: 256055

Becton Dickinson & Co.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Becton Dickinson & Co. · 7 Loveton Cir · Sparks, MD · 21152-9212

Is this the product you have?

  • BD Veritor System Reader -In Vitro Diagnostic for use with BD Veritor
  • System Test Kit Devices Catalog Number256055
Lot codes and dates
  • Serial NumbersSerial Number

    124 of 124 codes

    • 1801179131J10
    • 1801179119J10
    • 1801179139J10
    • 1801179117J10
    • 1801179110J10
    • 1801179115J10
    • 1801159055J10
    • 1801179120J10
    • 1801159036J10
    • 1801179109J10
    • 1801179095J10
    • 1801179128J10
    • 1801189173J10
    • 1801189181J10
    • 1801189108J10
    • 1801189146J10
    • 1801189140J10
    • 1801189126J10
    • 1801189184J10
    • 1801189159J10
    • 1801179092J10
    • 1801179137J10
    • 1612139044GR0
    • 1801179121J10
    • 1801179124J10
    • 1801179148J10
    • 16102993246N0
    • 1801159030J10
    • 1801189102J10
    • 1801189132J10
    • 1801189166J10
    • 1801169045J10
    • 1801169012J10
    • 1801169057J10
    • 1801169049J10
    • 1801169003J10
    • 1801179155J10
    • 1801179142J10
    • 1710169021HM0
    • 16102993166N0
    • 1801169001J10
    • 1801179096J10
    • 1801179111J10
    • 1801189176J10
    • 1801189177J10
    • 1801189180J10
    • 1801169005J10
    • 1801179094J10
    • 1801179175J10
    • 1801179113J10
    • 1801179125J10
    • 1801189104J10
    • 1801189073J10
    • 1801189082J10
    • 1801169018J10
    • 1801179157J10
    • 1801179162J10
    • 1801179156J10
    • 1801189158J10
    • 1801179105J10
Amount recalled
124

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Background calibration has the potential to cause false positive or false negative test results. An incorrect test result with the BD Veritor System could lead to possible misdiagnosis and inappropriate treatment

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 4, 2020 · Data as of Sep 19, 6:18 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.