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Becton Dickinson & Co. recalls BD MAX Instrument, catalog #441916 Product Usage: The BD MAX System, used in conjunction with the appropriate extra
Recalled July 10, 2013 · FDA recall Z-1662-2013 · Becton Dickinson &
Hazard
Electrical power module installed on some in vitro diagnostic instruments does not meet industry standards as labeled. · FDA Class III
Units
71 instruments
Sold at
Worldwide Distribution - USA Nationwide and in the countries of: Japan, Singapore, Hong Kong, China, Australia, Europe, and Chile.
Description
Electrical power module installed on some in vitro diagnostic instruments does not meet industry standards as labeled.
Product
BD MAX Instrument, catalog #441916 Product Usage: The BD MAX System, used in conjunction with the appropriate extraction kits and reagents is capable of automated amplification and detection of target nucleic acid sequences for use in clinical, industrial, and research settings.
Manufacturer(s)
Becton Dickinson & Co.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →