Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Up&Up loratadine orally disintegrating tablets Recalled by Ohm Laboratories, Inc. Due to Superpotent Drug: Out Of Specification (OOS) result for...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ohm Laboratories, Inc. directly.
Affected Products
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
Quantity: 34,488 boxes
Why Was This Recalled?
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ohm Laboratories, Inc.
Ohm Laboratories, Inc. has 23 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report