Reported May 22, 2019 · Terminated
BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with the BD Veritor System Test Devices. Catalog Number:…
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 Plus Analyzer- In-Vitro Diagnostic intended to use with the BD Veritor System Test Devices
- Catalog Number256066
- Lot codes and dates
- Serial NumbersSerial Number
1807138J1E0501710067J160C01703027J07FD01810268J2D3701710217J184701703027J084C01703307J0C6301710067J161901709187J123601710267J19D401710067J162301710067J161D01710067J161F01710067J162601807138J1E0B01609076J042701802138J07B401803298J110701802078J05D801704067J0DA001612166J070C01710257J18F501802028J044C01703167J0B0B01612026J070101710067J161101802058J052101811128J2FF501710067J162001710067J162701710237J185C01702147J04360
- Serial NumbersSerial Number
- Amount recalled
- 32 units
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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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