Over the weekend, Ranbaxy announced the voluntary recall of Nitrofurantoin capsules (Sales of US$4.1 mn and TRx of 0.56 mn units in 2008) from the US market. Ranbaxy believes the recalled drug (an antibiotic for the treatment of urinary tract infections) is “unlikely to produce any serious adverse health effects” implying a Class III FDA classification.
Ranbaxy’s recall of Nitrofurantoin capsules is the second product recall, following the Gabapentin recall in November 2007. In this instance, Ranbaxy (more…)