6 FDA recalls mention Common. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Common.
Reason Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Reason cGMP deviations
Reason CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Reason Microbial contamination
Reason Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain sibutramine and phenolphthalein
Reason Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain sibutramine and phenolphthalein
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.