FDAMarch 6, 2015device
BD FACSCalibur; Catalog Numbers 342973, 342975, 34976 In vitro Diagnostics Use.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The circuit breakers on some BD FACSCalibur instruments may have the incorrect rated amperage (20 amps instead of 2 amps) causing the circuit breaker to fail to open in an over-current situation.
What to do
FDA enforcement status: Terminated
Brands named
bd biosciences systems reagents
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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