FDA-Drug2026-01-21Class IIPROCESSING DEFECT
Claritin 20-count antihistamine recalled for rodent contamination at distributor
MOLDNationwide distribution
Stop using Claritin from Gold Star Distribution
Gold Star Distribution Inc. distributed Claritin 20-count tablets that were stored in conditions with rodent exposure and activity at their distribution center. The FDA found insanitary conditions that violate manufacturing standards. This affects all lots of this product distributed by Gold Star that are still within their expiration date.
- Check if your Claritin 20-count came from Gold Star Distribution (check packaging or contact retailer)
- Do not use the medication if distributed by Gold Star
- Return it to where you purchased it for a refund or replacement
- Contact your pharmacist or doctor if you have questions about your allergy medication
Hazard
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Sold states
US Nationwide.
Affected count
Unknown
Manufactured in
1000 Humboldt Ave N, Minneapolis, MN, United States
Products
Claritin, 20 Count, UPC: 655708016305
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0266-2026Don't want to check this manually?
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