Nature Throid, 3/4 Grain (48.75 mg) Thyroid USP [Liothyronine (T3) 6.75 mcg, Levothyroxine (T4) 28.5 mcg], packaged in a) 100-count bottles (NDC 64727-3302-1) and b) 1000-count bottles (NDC 64727-3302-2), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034

Class I - Dangerous
💊 Drugs Recalled: August 25, 2020 RLC Labs Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot #: 109242, Exp. Date 11/2022
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
RLC Labs Inc.
Reason for Recall:
Subpotent Drug: FDA analysis found product to be subpotent
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Nature Throid, 3/4 Grain (48.75 mg) Thyroid USP [Liothyronine (T3) 6.75 mcg, Levothyroxine (T4) 28.5 mcg], packaged in a) 100-count bottles (NDC 64727-3302-1) and b) 1000-count bottles (NDC 64727-3302-2), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034

Product Codes/Lot Numbers:

Lot #: 109242, Exp. Date 11/2022

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-1616-2020

Related Recalls

CGMP Deviations: manufactured under the same conditions as those found to be subpotent.

Aug 25, 2020 Prescription Drugs Nationwide View Details →

CGMP Deviations: manufactured under the same conditions as those found to be subpotent.

Aug 25, 2020 Prescription Drugs Nationwide View Details →