DrugOct 21, 2015
Ohm Laboratories Sunmark loratadine Orally Disintegrating Tablets, USP, 10 mg recall — FDA D-0037-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
Recall history in this database
Classification mix: Class III: 13.
DrugOct 21, 2015
Ohm Laboratories Safeway Care Loratadine Orally Disintegrating Tablets, USP, 10 mg recall — FDA D-0034-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS, , USP, 10 mg recall — FDA D-0035-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories Discount Drug Mart Food Fair, Original Prescription Strength, Loratadine recall — FDA D-0024-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories Wal-itin Loratadine Orally Disintegrating Tablets, USP, 10 mg recall — FDA D-0038-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories CareOne Original Prescription Strength, Allergy Relief, Loratadine Orally recall — FDA D-0022-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories QC Quality Choice Loratadine Orally Disintegrating Tablets, USP 10 mg recall — FDA D-0019-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories Good Neighbor Pharmacy Loratadine Orally Disintegrating Tablets, USP, 10 mg recall — FDA D-0027-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories CVS Pharmacy, Original Prescription Strength, LORATADINE ORALLY recall — FDA D-0023-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories Rite Aid Pharmacy loratadine orally disintegrating tablets USP, 10 mg recall — FDA D-0020-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories Equaline Original Prescription Strength, loratadine orally disintegrating recall — FDA D-0025-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugOct 21, 2015
Ohm Laboratories Premier Value Loratadine Orally Disintegrating Tablets, USP, 10 mg recall — FDA D-0033-2016
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
DrugJun 24, 2015
Ohm Laboratories Loratadine Orally Disintegrating Tablets USP, 10 mg, Antihistamine, Allergy recall — FDA D-1142-2015
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Class IIIFDA: TerminatedOhm Laboratories, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Ohm Laboratories, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.