SWAN — Class I drug recall D-1507-2022
Terminated recall by Vi-Jon, LLC, reported 2022-09-21, distributed nationwide. Microbial contamination of non-sterile products.
| Recall number | D-1507-2022 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vi-Jon, LLC, Smyrna, TN, United States |
| Recall initiated | 2022-07-15 |
| Classified | 2022-09-09 |
| Reported by FDA | 2022-09-21 |
| Terminated | 2024-05-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, PA |
| Quantity | 27,612 bottles |
| Reason classes | microbial contamination, sterility |
| UPC / GTIN / UDI-DI | 00072785134058 |
| NDC | 00869-0166-38 |
| Lot numbers | 0562243 |
| Expiration dates | 2024-02-17 |
Product
SWAN, Citroma MAGNESIUM CITRATE, Saline Laxative, Oral Solution, (1.745 g/fl oz), Lemony Flavor, 10 FL OZ (296 mL), Distributed by: Vi-Jon, Inc. One Swan Drive Smyrna, TN 37167; NDC 0869-0166-38 UPC 0 72785 13405 8
Reason for recall
Microbial contamination of non-sterile products.
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-1507-2022. 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.