Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Sichuan Friendly Pharmaceutical Co.,Ltd.: Thyroid Powder Recalled Due to Inconsistent Active Ingredient Levels

Agency Publication Date: September 28, 2018
Share:
Sign in to monitor this recall

Summary

Sichuan Friendly Pharmaceutical Co.,Ltd. is recalling approximately 2,662 kilograms of Thyroid Powder (US Pharmacopoeia grade) because of deviations from current Good Manufacturing Practices (CGMP). The affected powder has been found to have inconsistent levels of the active ingredients levothyroxine and liothyronine. This thyroid medication ingredient was distributed nationwide across the United States and also in China.

Risk

Inconsistent levels of active thyroid hormones can lead to patients receiving too much or too little medication. This can cause significant health complications, including either symptoms of hypothyroidism (underactive thyroid) or hyperthyroidism (overactive thyroid), which may require medical intervention to stabilize.

What You Should Do

  1. Identify if you have the affected Thyroid Powder 25kg/drum by checking for NDC 7807-0170-11 and the manufacturer Sichuan Friendly Pharmaceutical Co., LTD.
  2. Check the packaging for the following lot numbers: 160601, 160602, 160603, 160801, 161101, 162011, 170301, 170501, 170502, 170701, and 170702.
  3. If you are a consumer using medication that may contain this ingredient, do not stop taking your medication; instead, contact your healthcare provider or pharmacist immediately for guidance and to discuss alternative treatments.
  4. Pharmacy and distribution facilities should immediately quarantine any unused product and contact the manufacturer at +886 832 2240082 or +886 832 2240298 for further instructions and potential return.
  5. Return any unused product to the pharmacy or place of purchase for a refund.
  6. Contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

๐Ÿ’ฐFull Refund

Return for refund and healthcare consultation

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund.

Affected Products

Product: Thyroid Powder 25kg/drum, US Pharmacopoeia
Model:
NDC 7807-0170-11
Recall #: D-0006-2019
Lot Numbers:
160601
160602
160603
160801
161101
162011
170301
170501
170502
170701
170702

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 80892
Status: Resolved
Manufacturer: Sichuan Friendly Pharmaceutical Co.,Ltd.
Sold By: Distributors in the United States and China
Manufactured In: China
Units Affected: 2662 kg
Distributed To: Nationwide
Agency Last Updated: October 2, 2018

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.