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Lower risk Drug recall · FDA · Published August 21, 2018

Sichuan Friendly Pharmaceutical Thyroid Powder Recall: Inconsistent Active Ingredients

Sichuan Friendly Pharmaceutical recalls Thyroid Powder 25kg/drum (NDC 7807-0170-11) due to inconsistent levothyroxine and liothyronine levels. Affected lots include 160601-170702. Consumers should check their lot numbers and contact the manufacturer.

🇺🇸 FDA recall #D-0006-2019DrugSichuan Friendly Pharmaceutical ›
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Recalling firmSichuan Friendly Pharmaceutical Co.,Ltd.No. 680 Hongpai Road, Dongxing · Neijiang, China
✎ GovInfoNow plain-language explainer

What happened, in plain English

Sichuan Friendly Pharmaceutical is recalling Thyroid Powder 25kg drums because the active ingredients levothyroxine and liothyronine levels are inconsistent. This could lead to improper thyroid medication dosing, which may cause health issues if the medication is not taken correctly. Read more at govinfonow.com/recall/39701-sichuan-friendly-pharmaceutical-thyroid-powder-recall-inconsistent-active-ingredients.

Source Summary by GovInfoNow · govinfonow.com/recall/39701-sichuan-friendly-pharmaceutical-thyroid-powder-recall-inconsistent-active-ingredients · Updated October 6, 2026 · FDA enforcement record: FDA #D-0006-2019

Cite this page

“Sichuan Friendly Pharmaceutical Thyroid Powder Recall: Inconsistent Active Ingredients.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39701-sichuan-friendly-pharmaceutical-thyroid-powder-recall-inconsistent-active-ingredients. Based on FDA recall #D-0006-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0006-2019%22&limit=1).

Why it’s dangerous

The Thyroid Powder contains inconsistent levels of levothyroxine and liothyronine, the active ingredients for thyroid medication. This inconsistency means the medication may not provide the correct dose, potentially leading to improper treatment.

Who’s affected

People who have purchased Thyroid Powder 25kg drums with the specified lot numbers (160601-170702) from the manufacturer. Those using this medication for thyroid treatment are most at risk of incorrect dosing.

How to tell if you have this one

Check the lot number on the drum, which should be one of 160601, 160602, 160603, 160801, 161101, 162011, 170301, 170501, 170502, 170701, or 170702. The product is labeled as Thyroid Powder 25kg/drum with NDC 7807-0170-11.

  • Brand
    Sichuan Friendly Pharmaceutical
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Lot Number

    Look for the lot number on the drum, which should be one of the specified dates (160601-170702).

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Distributed nationwide and China” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 6.9 years after the firm started it.

1. Firm started the recall: Aug 21, 201812. FDA classified it Class II: Oct 2, 201823. Published in FDA’s Enforcement Report: Oct 10, 201834. FDA terminated the recall: Jul 7, 2025420182025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0006-2019 (August 21, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0006-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA