Medaus Pharmacy recalls 100mL Magnesium Chloride 200 mg/mL PF due to potential microbial contamination. Products may not be sterile, posing health risks. Contact 1-800-526-9183 for details.
Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.
Medaus Pharmacy is recalling a specific magnesium chloride solution because lab tests found it might not be sterile. This could lead to infections if someone uses it.
The product may contain harmful bacteria because lab tests showed microbial contamination. The FDA is concerned the lab that tested it might not have been reliable, so the product's sterility can't be guaranteed.
People who bought the Magnesium Chloride 200 mg/mL PF solution from Medaus Pharmacy between certain dates. Those using the product for medical purposes are most at risk.
Check the product label for 'Magnesium Chl 200 mg/mL PF, 100 mL' and the lot number 130307-60 (expired 9/3/2013). This product was sold through Medaus Pharmacy.
Look for the product name and lot number 130307-60 on the label.
The product may not be sterile due to lab tests showing microbial contamination, and the FDA is concerned the testing lab might not be reliable.
Check the label for 'Magnesium Chl 200 mg/mL PF, 100 mL' and lot number 130307-60 (expired 9/3/2013).
The recall record does not specify a remedy, so contact Medaus Pharmacy at 1-800-526-9183 for further instructions.
We’ve drafted a message you can send Medaus to request your refund or repair — edit it as you like.
Subject: Recall D-1053-2013 — Medaus Medaus Hello, I own a Medaus that is covered by recall D-1053-2013 from Medaus. 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.
