Ohm Loratadine Orally Disintegrating Tablets recall: Superpotent
Ohm Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets, Distributed by Ohm Laboratories, Inc. 1385 Livingston Avenue, North Brunswick, NJ 08902, NDC 51660-527-31, UPC 3 5166052731 5
Why was Ohm Loratadine Orally Disintegrating Tablets recalled?
Superpotent Drug: Out Of Specification (OOS) result for Assay.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Batch Numbers: 2544486, Exp 7/31/2016; 2617891, Exp 5/31/2016; 2644272, Exp 9/30/2016
- Product
- Ohm Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets, Distributed by Ohm Laboratories, Inc. 1385 Livingston Avenue, North Brunswick, NJ 08902, NDC 51660-527-31, UPC 3 5166052731 5
- Recalling firm
- Ohm Laboratories, Inc.
- Quantity
- 311 boxes
- Distribution
- Nationwide.
- Recall date
- October 21, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)