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Becton Dickinson & Co. recalls BD MAX DNA MMK Lab Use, catalog no. 442828
Recalled May 9, 2018 · FDA recall Z-1545-2018 · Becton Dickinson &
Hazard
The package insert incorrectly lists the volume of the primer and probe diluent to use for the reconstitution of the master mix tube. Adding the incorrect amount of diluent could have an effect on the assay. · FDA Class III
Units
N/A
Sold at
Distributed to accounts in 8 states: CA, FL, NJ, NY, OR, PA, VA, and WI. International distribution to Argentina, Australia, Brazil, Canada, Chile, China, Colombia, Europe, Hong Kong, Japan, Singapore, Taiwan, and Thailand.
Description
The package insert incorrectly lists the volume of the primer and probe diluent to use for the reconstitution of the master mix tube. Adding the incorrect amount of diluent could have an effect on the assay.
Product
BD MAX DNA MMK Lab Use, catalog no. 442828
Manufacturer(s)
Becton Dickinson & Co.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →