Drug & medication recalls

Ohm Laboratories, Inc. recalls QC Quality Choice Loratadine Orally Disintegrating Tablets, USP 10 mg, 10-count tablets per box, Distributed by C.D.M.A…

Recall date
July 28, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
D-0019-2016
FDA classification
Class III
Brand / firm
Ohm Laboratories, Inc.
Sold / distributed
Nationwide.

Why it was recalled

Superpotent Drug: Out Of Specification (OOS) result for Assay.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

QC Quality Choice Loratadine Orally Disintegrating Tablets, USP 10 mg, 10-count tablets per box, Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376-0995, NDC 63868-157-10, UPC 6 35515 95777 0

Get recall alerts

Free email alert whenever Ohm Laboratories, Inc. has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Ohm Laboratories, Inc.