34 FDA recalls mention Loratadine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Loratadine.
Reason Superpotent Drug: Out Of Specification (OOS) result for Assay.
Reason Superpotent Drug: Out Of Specification (OOS) result for Assay.
Reason Presence of Foreign Substance: Presence of blue plastic floating in loratadine syrup.
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
Reason Defective Container: An unacceptable level of blister defects have been identified in Loratadine and Pseudoephedrine Sulfate Extended Release…
Reason Failed Tablet/Capsule Specifications: Affected lot numbers may contain chipped or broken tablets.
Reason Failed Tablet/Capsule Specifications: The products are being recalled due to chipped and broken tablets.
Reason Labeling: Label Mixup: DESLORATADINE, Tablet, 5 mg may have potentially been mislabeled as the following drug: ASCORBIC ACID, Tablet, 250 mg, NDC…
Reason Labeling: Label Mixup; LORATADINE Tablet, 10 mg may be potentially mislabeled as GLYCOPYRROLATE, Tablet, 2 mg, NDC 00603318121, Pedigree: W002650…
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