Beaumont Bio-med Recalls Skin Irritation Spray Due to Contamination Risk
Beaumont Bio-med recalls 192 bottles of Skin Irritation & Itch Response Homeopathic Formula due to potential microbial contamination from CGMP deviations.
Use caution until it’s fixed
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Contact the company
What happened, in plain English
Beaumont Bio-med, Inc. is recalling a small quantity of its Skin Irritation & Itch Response Homeopathic Formula because it was manufactured under conditions that could lead to microbial contamination. The recall affects 192 bottles distributed nationwide in the USA. The company has not provided specific instructions for consumers on what to do with the product at this time. Read more at govinfonow.com/recall/39662-beaumont-bio-med-recalls-skin-irritation-spray-due-to-contamination.
Source Summary by GovInfoNow · govinfonow.com/recall/39662-beaumont-bio-med-recalls-skin-irritation-spray-due-to-contamination · Updated October 11, 2026 · FDA enforcement record: FDA #D-1192-2018
Cite this page
“Beaumont Bio-med Recalls Skin Irritation Spray Due to Contamination Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/39662-beaumont-bio-med-recalls-skin-irritation-spray-due-to-contamination. Based on FDA recall #D-1192-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1192-2018%22&limit=1).
Why it’s dangerous
The product was manufactured by a contract manufacturer under conditions that deviated from Current Good Manufacturing Practices (CGMP). These deviations create a possibility of microbial contamination in the oral spray, which could pose a health risk if ingested or applied to irritated skin.
Who’s affected
Consumers who purchased the Skin Irritation & Itch Response Homeopathic Formula from retailers across the United States between the production dates and expiration dates listed. Individuals using the spray for skin irritation or itch relief are at risk of exposure to potential microbial contaminants.
How to tell if you have this one
Check your bottle for the following details: Brand is Beaumont Bio-med; Product is Skin Irritation & Itch Response Homeopathic Formula; Size is 2 FL. OZ. (59.2 mL) in an amber glass oral spray bottle; NDC is 58066-7002-7. Verify the lot number and expiration date: Lot 091515C expires 09/2018, or Lot 050118S expires 05/2021.
- Brand
Beaumont Bio-med- Category
Drug
All 8 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Nationwide in the USA
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1192-2018 | Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7002-7; Lot: 091515C, Exp 09/2018; 050118S, Exp 05/2021 | 192 bottles |
| D-1193-2018 | Sinus Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7013-7; Lot: 100316A, Exp 10/2019 | 90 bottles |
| D-1194-2018 | Sore Throat & Laryngitis Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7014-7; Lot: 100316G, Exp 10/2019; 050118R, Exp 05/2021 | 420 bottles |
| D-1195-2018 | Diarrhea Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7022-7; Lot: 090915A, Exp 09/2018 | 160 bottles |
| D-1196-2018 | Muscle & Joint Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7041-7; Lot: 012916F, Exp 01/2019 | 109 bottles |
| D-1197-2018 | Allergy & Hay Fever Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7011-7; Lot: 050216X, Exp 05/2019 | 124 bottles |
| D-1198-2018 | Colds & Flu Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7012-7; Lot: 042816C, Exp 04/2019; 112317K, Exp 11/2020 | 314 bottles |
| D-1199-2018 | Arthritis Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7042-7; Lot: 012916E, Exp 01/2019 | 140 bottles |
What to do — step by step
Check Your Bottle
Verify if your product matches the NDC 58066-7002-7 and lot numbers 091515C or 050118S.
Monitor for Updates
Since no specific remedy is currently stated, watch for official updates from Beaumont Bio-med regarding returns or disposal instructions.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 4 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
How many bottles are being recalled?
A total of 192 bottles are included in this recall.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1192-2018 (August 31, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1192-2018 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.