Class II · Moderate risk Terminated
Desloratadine Tablets USP 5mg a) 100 count
Reason CGMP Deviations: N-Nitroso Desloratadine impurity result exceeded the acceptable intake limit.
Rite Aid Pharmacy loratadine orally disintegrating tablets USP
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Superpotent Drug: Out Of Specification (OOS) result for Assay.
What was recalled
Rite Aid Pharmacy loratadine orally disintegrating tablets USP, 10 mg, packaged in a) 30-count tablets per box, Item 352712, UPC 0 11822 52712 5; b) 60-count tablets per box, Item 353672, UPC 0 11822 53672 1. Distributed By: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011.
- Recalling firm
- Ohm Laboratories, Inc.
- Origin
- NJ, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0020-2016
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Loratadine recalls
See all
Class II · Moderate risk Ongoing
Claritin Allergy Liq Chldrns Grape 2 Floz Sku 900834 Claritin…
Reason CGMP Deviations: product held outside appropriate storage temperature conditions.
Class III · Low risk Terminated
AllerClear D-24 hr
Reason Failed Moisture Limits
Class III · Low risk Terminated
Loratadine-D Extended-Release Tablets
Reason Failed Moisture Limits
Class II · Moderate risk Terminated
Children's Loratadine Oral Solution USP
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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