Vi-Jon recalls Magnesium Citrate Saline Laxative Oral Solution due to CGMP deviations. Affected products include specific UPCs and retailers. No remedy provided in official notice.
CGMP Deviations
Vi-Jon is recalling a specific magnesium citrate laxative solution because of manufacturing quality control issues. This recall affects certain products sold under specific UPC codes and retailers. The product is not safe to use as it may pose a risk to consumers.
The product was manufactured with deviations from current Good Manufacturing Practices (CGMPs). This means the product may not meet safety and quality standards, potentially leading to health risks if consumed.
Owners of the recalled Magnesium Citrate Saline Laxative Oral Solution with the listed UPCs or NDCs are affected. People using this product for bowel movements may be at risk due to the manufacturing issues.
Check the product label for the UPC codes listed: Best Choice UPC 0 70038, Careone UPC 3 41520 00055, CVS Health UPCs, and other specific NDCs and UPCs mentioned in the recall notice.
Look for the specific UPC or NDC codes listed in the recall notice to confirm if your product is affected.
The official recall notice does not provide any remedy steps.
The product was manufactured with deviations from current Good Manufacturing Practices (CGMPs), which may affect its safety and quality.
The product was sold through retailers including Best Choice, Careone, CVS, Walgreens, and others with specific UPCs and NDCs listed in the recall notice.
We’ve drafted a message you can send Vi-Jon to request your refund or repair — edit it as you like.
Subject: Recall D-1512-2022 — Vi-Jon Vi-Jon Hello, I own a Vi-Jon that is covered by recall D-1512-2022 from Vi-Jon. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.