Reported Jul 10, 2013 · Terminated
BD MAX Instrument, catalog #441916 Product Usage: The BD MAX System, used in conjunction with the appropriate…
Becton Dickinson & Co.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.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. · BD Diagnostic Systems · Sparks, MD · 21152-0999
Is this the product you have?
- BD MAX Instrument, catalog #441916
- Product UsageThe 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
- Lot codes and dates
- Serial Numbers
CT0173 to CT0249CT0253 to CT0260CT0262CT0263CT0265CT0269and CT0272
- Serial Numbers
- Amount recalled
- 71 instruments
Where it was sold
- Nationwide
Why it was recalled
Electrical power module installed on some in vitro diagnostic instruments does not meet industry standards as labeled.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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