Boric Acid 600 mg per suppository — Class II drug recall D-1184-2022
Terminated recall by Wedgewood Village Pharmacy, LLC, reported 2022-07-13, distributed nationwide. Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection
| Recall number | D-1184-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wedgewood Village Pharmacy, LLC, Swedesboro, NJ, United States |
| Recall initiated | 2022-06-10 |
| Classified | 2022-07-07 |
| Reported by FDA | 2022-07-13 |
| Terminated | 2023-02-16 |
| Distributed | Nationwide (US) |
| Quantity | 14 suppositories |
| Lot numbers | 000-03843532 |
| Expiration dates | 2022-09-06 |
Product
Boric Acid 600 mg per suppository, 14 Vaginal Suppositories per box, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085
Reason for recall
Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection
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-1184-2022. 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.