FDA Recall
Terminated
Historical recordClass III
Meijer Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box, Dist. By Meijer Distribution Inc. 2929 Walker Avenue NW, Grand Rapids, MI 49544. NDC 41250-527-31, UPC 7 6023662291 8
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Wal-itin Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-coiunt tablets per box, (NDC 0363-0527-69, ITEM 367492,UPC 3 1191717021 3); and b) 30-count tablets per box, (NDC 0363-0527-31, ITEM 254166, UPC 3 191715562 ) Distributed by Walgreen Co., 200 Wilmot Road, Deerfield, IL 60015
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Sunmark loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box (NDC 49348-930-01, UPC 0 1093936544 6); and b) 30-count tablets per box (NDC 49348-930-44, UPC 0 1093934944 6) Distributed by McKesson, One Post Street, San Francisco, CA 94104
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
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
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS, , USP, 10 mg, packaged in a) Children's 10-count tablets per box (NDC 36800-528-69, UPC 0 3680010261 3); and b) 10-count tablets per box, (NDC 36800-527-69, UPC 0 3680008395 0); Distributed by Topco Associates, LLC, Elk Grove Village, IL 60007.
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Safeway Care Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box (NDC 21130-527-69, UPC 3 2113076240 9); b) 30-count tablets per box (NDC 21130-527-31, UPC 3 2113076252 2) Distributed by Safeway Inc. PO BOX 99, Pleasanton, CA 94566
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Premier Value Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box; Distributed by Chain Drug Consortium, 3301 NW Boca Raton Blvd. Suite 101, Boca Raton, FL 33431, NDC 68016-527-31, UPC 8 4098601899 2
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
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
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Major loratadine orally disintegrating tablets, USP, 10 mg, 10-count tablets per box, Distributed by Major Pharmaceuticals 31778 Enterprise Drive, Livonia, MI 48150, USA, NDC 0904-5806-15, UPC 3 0904580615 9
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Leader Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box, Distributed by Cardinal Health, Dublin, OH 43017, NDC 37205-745-65, UPC 0 9629512322 7
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
HEB Loratadine Orally Disintegrating Tablets, USP, 10 mg, 10-count tablets per box, Made with pride & care for HEB, San Antonio, TX 78204, Item code: 188330, UPC 0 4122081968 3
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Health Mart Pharmacy loratadine orally disintegrating tablets, USP, 10 mg, 10-count tablets per box, Distributed by: McKesson, One Post Street, San Francisco, CA 94104, NDC 62011-0073-1, UPC 0 5256913369 9
by Ohm Laboratories, Inc.
- Reason
- Superpotent Drug: Out Of Specification (OOS) result for Assay.
- Published
- October 21, 2015
- Distribution
- Nationwide
View recall →
This page lists recalls that name Ohm Laboratories, Inc. as the recalling firm in the official source notice. It is
not a safety rating, ranking, or statement that the company acted negligently.
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