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Beaumont Bio Med, Inc. Issues Voluntary Nationwide Recall of all their Homeopathic Aqueous/Alcohol-Based Medicines due to the Nationwide Recall by the Contract Manufacturer, King Bio, of all their Aqueous-Based Products due to Possible Microbial Contamination

Audience: Consumer, Health Professional, Pharmacy

Beaumont Bio Med, Inc. is voluntarily recalling its entire aqueous/alcohol-based product line for human use, within expiry, to the consumer level. All products manufactured by the contract manufacturer, King Bio, have been recalled due to possible microbial contamination.

Risk Statement: The administration or use of drug products with microbial contamination could potentially result in increased infections that may require medical intervention, and could result in infections that could be life threatening to certain individuals. To date, Beaumont Bio Med has not received any reports of adverse events related to this recall.

The products being recalled are listed in this table: 

Products NameSize/Packaging/Dosage FormNDC NumberLot NumberExpire Date
Skin Irritation & Itch Response2 Fl Oz, Amber Glass, Oral Spray58066 7002 7091515C09/2018
Skin Irritation & Itch Response2 Fl Oz, Amber Glass, Oral Spray58066 7002 7050118S05/2021
Sinus Response2 Fl Oz, Amber Glass, Oral Spray58066 7013 7100316A10/2109
SoreThroat & Laryngitis Response2 Fl Oz, Amber Glass, Oral Spray58066 7014 7100316G10/2019
SoreThroat & Laryngitis Response2 Fl Oz, Amber Glass, Oral Spray58066 7014 7050118R05/2021
Diarrhea Response2 Fl Oz, Amber Glass, Oral Spray58066 7022 709091509/2018
Muscle & Joint Pain Relief2 Fl Oz, Amber Glass, Oral Spray58066 7041 7012916F01/2019
Allergy & Hay Fever Relief2 Fl Oz, Amber Glass, Oral Spray58066 7011 7050216X05/2019
Cold & Flu Response2 Fl Oz, Amber Glass, Oral Spray58066 7012 7042816C04/2019
Cold & Flu Response2 Fl Oz, Amber Glass, Oral Spray58066 7012 7112317K11/2020
Arthritis Pain Relief2 Fl Oz, Amber Glass, Oral Spray58066 7042 7112317K01/2019

Beaumont Bio Med Homeopathic Medicines are distributed Nationwide in the USA to wholesalers, health professionals and retail establishments and on our website www.naturalief.com.

Beaumont Bio Med is notifying its distributors and customers by email and/or phone and is arranging for return/replacement/refund of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using, discard or return to place of purchase for replacement or refund.

Consumers with questions regarding this recall can contact Beaumont Bio Med by phone : 800-332-2249 or e-mail: recall@naturalief.com on Monday – Friday from 8:30AM to 4:00PM, CDT. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Adverse reactions or quality problems associated with the use of this product may be reported to FDA's MedWatch Adverse Event Reporting program either by phone, on line, by regular mail or by fax.

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