Dr. King's Safecare+ AsthmaCare Homeopathic, Not a Rescue Inhaler, 2 fl oz (59 mL), UPC 357955404422, NDC 57955-4044-1

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

What Should You Do?

  1. Check if you have this product:
    Lots: 122216K Exp. 12/19; 120217P Exp. 12/19; 111117C Exp. 11/19; 083116C Exp. 08/19; 082316E Exp. 08/19; 072015A Exp. 07/18; 062716C Exp. 06/19; 062316B Exp. 06/19; 062218C Exp. 06/20; 052218C Exp. 05/20; 052118C Exp. 05/20; 051716J Exp. 05/19; 041816C Exp. 04/19; 030316A Exp. 03/19; 022317H Exp. 02/20; 111516H Exp. 11/19; 091815A Exp. 09/18; 062718C Exp. 06/20; 081815A Exp. 08/18
  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:

Dr. King's Safecare+ AsthmaCare Homeopathic, Not a Rescue Inhaler, 2 fl oz (59 mL), UPC 357955404422, NDC 57955-4044-1

Product Codes/Lot Numbers:

Lots: 122216K Exp. 12/19; 120217P Exp. 12/19; 111117C Exp. 11/19; 083116C Exp. 08/19; 082316E Exp. 08/19; 072015A Exp. 07/18; 062716C Exp. 06/19; 062316B Exp. 06/19; 062218C Exp. 06/20; 052218C Exp. 05/20; 052118C Exp. 05/20; 051716J Exp. 05/19; 041816C Exp. 04/19; 030316A Exp. 03/19; 022317H Exp. 02/20; 111516H Exp. 11/19; 091815A Exp. 09/18; 062718C Exp. 06/20; 081815A Exp. 08/18

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0909-2019

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