Party Relief — Class II drug recall D-0116-2019
Terminated recall by Sprayology, reported 2018-11-07, distributed nationwide. CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible
| Recall number | D-0116-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sprayology, Gaithersburg, MD, United States |
| Recall initiated | 2018-10-09 |
| Classified | 2018-10-30 |
| Reported by FDA | 2018-11-07 |
| Terminated | 2019-04-18 |
| Distributed | Nationwide (US) |
| Quantity | 2,956 bottles |
| Reason classes | microbial contamination, cgmp |
| NDC | 61096-0030-01, 61096-1030-01 |
Product
Party Relief, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0030-1 and Tester NDC 61096-1030-1
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-0116-2019. 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.