Skin Irritation & Itch Response Homeopathic Formula — Class II drug recall D-1192-2018
Terminated recall by Beaumont Bio-med, Inc., reported 2018-09-26, distributed nationwide. CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible
| Recall number | D-1192-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beaumont Bio-med, Inc., Waukon, IA, United States |
| Recall initiated | 2018-08-31 |
| Classified | 2018-09-17 |
| Reported by FDA | 2018-09-26 |
| Terminated | 2022-09-16 |
| Distributed | Nationwide (US) |
| Quantity | 192 bottles |
| Reason classes | microbial contamination, cgmp |
| NDC | 58066-7002-07 |
| Lot numbers | 050118S, 091515C |
| Expiration dates | 2018-09, 2021-05 |
Product
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
Reason for recall
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1192-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.