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Medium RiskFDA Drug
Medications & Supplements/Over-the-Counter

Beaumont Bio-med, Inc.: Homeopathic Oral Sprays Recalled Due to Potential Microbial Contamination

Agency Publication Date: September 17, 2018
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Summary

Beaumont Bio-med, Inc. is recalling approximately 1,549 bottles of eight different homeopathic oral spray formulas, including products for skin irritation, sinus issues, sore throats, and pain relief. The recall was initiated because the products were manufactured by a contract manufacturer under conditions that could lead to microbial contamination. Consumers who use these products should be aware that contaminated medications can cause infections, particularly in vulnerable populations. These items were sold in 2 FL. OZ. (59.2 mL) amber glass oral spray bottles nationwide. If you have these products, you should contact your healthcare provider or pharmacist and return the items for a refund.

Risk

The products may have been manufactured in an environment that allows for microbial contamination. If a contaminated product is used as an oral spray, it could introduce harmful bacteria or pathogens into the body, potentially leading to serious infections.

What You Should Do

  1. Check your medicine cabinet for 2 FL. OZ. (59.2 mL) amber glass oral spray bottles labeled as Skin Irritation & Itch Response, Sinus Response, Sore Throat & Laryngitis Response, Diarrhea Response, Muscle & Joint Pain Relief, Allergy & Hay Fever Relief, Colds & Flu Response, or Arthritis Pain Relief.
  2. Verify the Lot and Expiration dates on your bottles: Skin Irritation (Lot 091515C Exp 09/2018 or 050118S Exp 05/2021); Sinus (Lot 100316A Exp 10/2019); Sore Throat (Lot 100316G Exp 10/2019 or 050118R Exp 05/2021); Diarrhea (Lot 090915A Exp 09/2018); Muscle & Joint (Lot 012916F Exp 01/2019); Allergy (Lot 050216X Exp 05/2019); Colds & Flu (Lot 042816C Exp 04/2019 or 112317K Exp 11/2020); and Arthritis (Lot 012916E Exp 01/2019).
  3. Stop using the recalled homeopathic sprays immediately to avoid the risk of infection.
  4. Contact your healthcare provider or pharmacist if you have used any of these products and have concerns about your health.
  5. Return any unused product to the place of purchase for a full refund.
  6. For further instructions, contact Beaumont Bio-med, Inc. at their distribution location in Waukon, Iowa.
  7. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare consultation and refund.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Skin Irritation & Itch Response Homeopathic Formula (2 FL. OZ.)
Model:
NDC 58066-7002-7
D-1192-2018
Lot Numbers:
091515C (Exp 09/2018)
050118S (Exp 05/2021)
Date Ranges: September 2018, May 2021
Product: Sinus Response Homeopathic Formula (2 FL. OZ.)
Model:
NDC 58066-7013-7
D-1193-2018
Lot Numbers:
100316A (Exp 10/2019)
Date Ranges: October 2019
Product: Sore Throat & Laryngitis Response Homeopathic Formula (2 FL. OZ.)
Model:
NDC 58066-7014-7
D-1194-2018
Lot Numbers:
100316G (Exp 10/2019)
050118R (Exp 05/2021)
Date Ranges: October 2019, May 2021
Product: Diarrhea Response Homeopathic Formula (2 FL. OZ.)
Model:
NDC 58066-7022-7
D-1195-2018
Lot Numbers:
090915A (Exp 09/2018)
Date Ranges: September 2018
Product: Muscle & Joint Pain Relief Homeopathic Formula (2 FL. OZ.)
Model:
NDC 58066-7041-7
D-1196-2018
Lot Numbers:
012916F (Exp 01/2019)
Date Ranges: January 2019
Product: Allergy & Hay Fever Relief Homeopathic Formula (2 FL. OZ.)
Model:
NDC 58066-7011-7
D-1197-2018
Lot Numbers:
050216X (Exp 05/2019)
Date Ranges: May 2019
Product: Colds & Flu Response Homeopathic Formula (2 FL. OZ.)
Model:
NDC 58066-7012-7
D-1198-2018
Lot Numbers:
042816C (Exp 04/2019)
112317K (Exp 11/2020)
Date Ranges: April 2019, November 2020
Product: Arthritis Pain Relief Homeopathic Formula (2 FL. OZ.)
Model:
NDC 58066-7042-7
D-1199-2018
Lot Numbers:
012916E (Exp 01/2019)
Date Ranges: January 2019

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 80963
Status: Resolved
Manufacturer: Beaumont Bio-med, Inc.
Sold By: Beaumont Bio-med, Inc.
Manufactured In: United States
Units Affected: 8 products (192 bottles; 90 bottles; 420 bottles; 160 bottles; 109 bottles; 124 bottles; 314 bottles; 140 bottles)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.