Warning
GOLD STAR DISTRIBUTION INC Recalls LIQUID DAYQUIL 12/8oz
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0268-2026Drug / Pharmaceutical
GOLD STAR DISTRIBUTION INC Recalls LIQUID DAYQUIL 12/8oz
GOLD STAR DISTRIBUTION INC · Class II — Moderate Risk
Product Description
LIQUID DAYQUIL 12/8oz
Reason for Recall
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
US Nationwide.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
GOLD STAR DISTRIBUTION INC has recalled a pharmaceutical product that the FDA classified as Class II. The recall was initiated on December 26, 2025. CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. It was distributed in US Nationwide. Class II recalls involve products that might cause a temporary health problem or pose only a slight threat of a serious nature. Consumers should discontinue use and contact the firm.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medical Product Contamination.