4 FDA recalls mention Loperamide. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Loperamide.
Reason CGMP Deviations: product held outside appropriate storage temperature conditions.
Reason cGMP deviations: Temperature abuse
Reason Labeling Not Elsewhere Classified: The front panel indicates 24 caplets whereas the side panel indicates 12 caplets. The drug product carton…
Reason Defective Container; damaged blister units
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