Drugs & medicalClass II

ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg), 90 Tablets bottles, Rx only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC…

Subpotent Drug

Read the official notice →
Date
2026-07-08
Country
United States
Brand
Accord Healthcare
Product
Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg), 90 Tablets bottles, Rx only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC…
Classification
Class II
Units
US Nationwide.
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Accord Healthcare recalls

  1. 2026-09-02
  2. US
  3. 2025-10-15
  4. US
    Drugs & medicalClass II

    ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 90 Tablets per bottle, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh,…

    Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved specification range.

    FDA · DrugACCORD HEALTHCARE, INC.Nationwide in the USOfficial notice →
  5. 2025-07-23
  6. US
    Drugs & medicalClass II

    ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC…

    Subpotent Drug: Assay below the approved specification

    FDA · DrugACCORD HEALTHCARE, INC.Nationwide in the USAOfficial notice →
  7. 2025-05-07
  8. US
  9. 2024-12-11
  10. US
  11. 2024-11-06
  12. US
    Drugs & medicalClass II

    ACCORD HEALTHCARE, INC. recalls Cinacalcet Tablets, 90 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-442-10, b) 90 Tablets per bottle, NDC: 16729-442-15,…

    CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.

    FDA · DrugACCORD HEALTHCARE, INC.Nationwide in the USA and PROfficial notice →
All 14 Accord Healthcare recalls →

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    FDA · DrugLannett Company Inc.US Nationwide.Official notice →
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    FDA · DrugBoehringer Ingelheim Pharmaceuticals, Inc.OHOfficial notice →
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    SUN PHARMACEUTICAL INDUSTRIES INC recalls Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm Laboratories, Inc.,…

    Failed Impurities/Degradation Specifications

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCU.S. NationwideOfficial notice →
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