NET Remedies #5 Fire Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4205-2

Class I - Dangerous
💊 Drugs Recalled: July 20, 2018 King Bio Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lots: NR-022318E Exp. 02/20; NR-030418A Exp. 03/20; NR-051618D Exp. 05/20; NR-051818D Exp. 05/20; NR-081017E Exp. 08/19; NR-120317E Exp. 12/19; NR-121517A Exp. 12/19; NR-031516J Exp. 3/19; NR-010617E Exp. 01/20; NR011216H Exp. 01/19; NR-040417C Exp. 4/20; NR-050916D Exp. 5/19; NR-061517A Exp. 6/20; NR-061616D Exp. 6/19; NR-080116A Exp. 8/19; NR090115J Exp. 9/18; NR-090916B Exp. 9/19; NR-101416E Exp. 10/19; NR-120815K Exp.12/18
  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:
King Bio Inc.
Reason for Recall:
Microbial contamination
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

NET Remedies #5 Fire Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4205-2

Product Codes/Lot Numbers:

Lots: NR-022318E Exp. 02/20; NR-030418A Exp. 03/20; NR-051618D Exp. 05/20; NR-051818D Exp. 05/20; NR-081017E Exp. 08/19; NR-120317E Exp. 12/19; NR-121517A Exp. 12/19; NR-031516J Exp. 3/19; NR-010617E Exp. 01/20; NR011216H Exp. 01/19; NR-040417C Exp. 4/20; NR-050916D Exp. 5/19; NR-061517A Exp. 6/20; NR-061616D Exp. 6/19; NR-080116A Exp. 8/19; NR090115J Exp. 9/18; NR-090916B Exp. 9/19; NR-101416E Exp. 10/19; NR-120815K Exp.12/18

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0945-2019

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