Vi-Jon recalls lemon-flavored magnesium citrate laxative oral solution due to microbial contamination. Products sold by Meijer with specific lot numbers are affected. Consumers should check labels for NDC 41250-708-38 and lot number 0557622.
Microbial contamination of non-sterile products.
Vi-Jon is recalling lemon-flavored magnesium citrate laxative oral solution because it may contain harmful microorganisms. This could lead to infections or illness if consumed. The affected products have specific lot numbers and were sold by Meijer.
The laxative solution may have been contaminated with harmful microorganisms during manufacturing. This contamination could cause infections or illness if the product is consumed. The risk is higher for individuals who use the product for bowel preparation procedures.
People who purchased the lemon-flavored magnesium citrate laxative oral solution from Meijer with the NDC code 412:50-708-38 and lot number 0557622 are affected. Those using the product for bowel preparation are at higher risk.
Check the label for the product name: 'Magnesium Citrate Saline Laxative, Oral Solution, Lemon Flavor, 10 FL OZ'. Look for the NDC code 41250-708-38 and lot number 0557622 on the packaging.
Look for the NDC code 41250-708-38 and lot number 0557622 on the product label.
The recall record states there is a risk of microbial contamination, so the product is not safe to use as recalled.
The recall record does not specify a remedy, so consumers should check the product label for the NDC code and lot number and contact Meijer for further instructions.
Check the product label for the NDC code 41250-708-38 and lot number 0557622. Products sold by Meijer with these identifiers are affected.
We’ve drafted a message you can send Vi-Jon to request your refund or repair — edit it as you like.
Subject: Recall D-1504-2022 — Vi-Jon Vi-Jon Hello, I own a Vi-Jon that is covered by recall D-1504-2022 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.
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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.
