EQUALINE magnesium citrate saline laxative — Class I drug recall D-1502-2022
Terminated recall by Vi-Jon, LLC, reported 2022-09-21, distributed nationwide. Microbial contamination of non-sterile products.
| Recall number | D-1502-2022 |
|---|---|
| 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 | 5,304 bottles |
| Reason classes | microbial contamination, sterility |
| UPC / GTIN / UDI-DI | 00041163500686 |
| NDC | 41163-0769, 41163-0769-38 |
| Lot numbers | 0511629 |
| Expiration dates | 2022-12-04 |
Product
EQUALINE magnesium citrate saline laxative, oral solution, (1.745 g/fl oz), DYE FREE lemon flavor, 10 FL OZ (296 mL), Distributed by Supervalu Inc. Eden Prairie, MN 55344 USA, or Distributed By UNFI Providence, RI 02908, NDC 41163-769-38 UPC 0 41163 50068 6
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-1502-2022. 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.