Boric Acid 600 mg capsules — Class II drug recall D-1183-2022
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-1183-2022 |
|---|---|
| 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 | 1 boxes |
| Lot numbers | 000-03868160 |
| Expiration dates | 2022-09-14 |
Product
Boric Acid 600 mg capsules, 14 capsules per box, Qty: 1, 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-1183-2022. 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.