FDAFDA · Food and drugs·Recall number D-0069-2022
AllerClear D-24 hr, (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10/240mg), 15-count blister packs, Manufactured by: Ohm Laboratories Inc., 1385 Livingston Avenue, North Brunswick, NJ 08902, NDC 63981-724-15
Published November 3, 2021 · Recall initiated: October 12, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Moisture Limits
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- KIRKLAND SIGNATURE ALLERCLEAR D 24 HR
- Manufacturer
- SUN PHARMACEUTICAL INDUSTRIES INC
- Distributor
- Nationwide within the United States
- Lot
- AC09723, Exo, Date 11/2022
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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