"SUNDIAL***TRADITIONAL HERBAL FORMULA***Flu-Allergies HayFever***" packaged in boxes

Sundial Herbal Products recalled "SUNDIAL***TRADITIONAL HERBAL FORMULA***Flu-Allergies HayFever***" packaged in boxes in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Jun 30, 2020.

The recall cites a labeling or packaging error: "Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims." Labeling defects matter most when the wrong label conceals an ingredient a consumer is trying to avoid.

Distribution was limited; the FDA record lists "NY." Single-area recalls still warrant a kitchen check for anyone who shops within that footprint. The recalling firm is based in Bronx, NY. The recall covers Unknown of product. The FDA has Terminated this recall (first reported Sep 9, 2020), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.