Moderate riskFDA DrugClass II

DayQuil Cold & Flu 2-pack recalled for insanitary conditions

DayQuil Cold & Flu 32-count twin packs distributed by Gold Star Distribution may have been stored in insanitary conditions with rodent activity at a distribution center. The FDA is recalling all lots still within their expiration date that were distributed nationwide.

From the FDA notice · Read the official notice ↗ · All Gold Star Distribution recalls

What to do

  1. Check if you have DayQuil Cold & Flu 32CT/2PK from Gold Star Distribution
  2. Stop using the product
  3. Throw away or return the medication to the store where you bought it
  4. Contact your pharmacist or doctor with questions

Is yours affected?

Compare your label or packaging with the recalled product.

Product
DAYQUIL COLD & FLU, 32CT/2PK
Sold in
Nationwide
Made for
Adults (0 months and older)

This recall covers 27 products — see all of them.

Details

Units affected
Unknown
Illnesses reported
None reported
Manufactured in
1000 Humboldt Ave N, Minneapolis, MN, United States
Classification
Class II
Recall number
D-0267-2026

In the FDA's words

Description
DAYQUIL COLD & FLU, 32CT/2PK CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. All lots within expiry distributed by Gold Star Distribution. Distribution: US Nationwide. Affected quantity: Unknown
Hazard
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

27 products in this recall

Advil, Tylenol and more OTC medicines recalled for rodent exposure

Gold Star Distribution is recalling 27 over-the-counter products, including pain relievers, cold and flu medicines, antacids, cough drops, skin and lip care, petroleum jelly, rubbing alcohol and mouthwash. The products were stored or distributed from a facility with insanitary conditions, including rodent exposure and activity. No injuries have been reported.

The agency lists each product separately. Check every one you might have.

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