Ohm Laboratories, Inc. recalls Up&Up loratadine orally disintegrating tablets, USP, 10 mg, 30-count tablets per box, Distributed by Target Corp, Minne
Recalled October 21, 2015 · FDA recall D-0036-2016 · Ohm Laboratories
Hazard
Superpotent Drug: Out Of Specification (OOS) result for Assay. · FDA Class III
Units
34,488 boxes
Sold at
Nationwide.
Description
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Product
Up&Up loratadine orally disintegrating tablets, USP, 10 mg, 30-count tablets per box, Distributed by Target Corp, Minneapolis, MN 55403; NDC 11673-527-31, UPC 3 5166052731 5
Manufacturer(s)
Ohm Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →