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Claritin, 20 Count, UPC: 655708016305

gold star distribution inc Claritin, 20 Count, UPC: 655708016305 recalled by FDA. CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

gold star distribution inc Claritin, 20 Count, UPC: 655708016305 recalled by FDA. CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source: FDA
Announced by source: December 26, 2025
Last reviewed by RecallRadar: March 4, 2026

What You Should Do

1## Claritin, 20 Count, UPC: 655708016305 Agency: FDA | Category: drug Reason: CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. What to do:
2Stop using the product if your lot/model matches.
3Check the FDA notice for specifics.
4Follow remedy instructions.

Open Official Recall Notice Get Alerts for gold star distribution inc Devices

What's Being Recalled

Quoted source excerpt from the official notice.

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

All lots within expiry distributed by Gold Star Distribution.

#	Model
1	All lots within expiry distributed by Gold Star Distribution.

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

Frequently Asked Questions

Is my gold star distribution inc device affected?

Check the affected models section on this page. The official notice currently lists All lots within expiry distributed by Gold Star Distribution..

What is the remedy for this recall?

## Claritin, 20 Count, UPC: 655708016305 Agency: FDA | Category: drug Reason: CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. What to do: 1. Stop using the product if your lot/model matches. 2. Check the FDA notice for specifics. 3. Follow remedy instructions.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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