Pharmedica USA recalls Purely Soothing 15% MSM Drops due to non-sterility risk. Affected products include 15ml and 30ml bottles with specific UPCs and lot numbers. Consumers should contact Pharmedica for details.
Non-Sterility
Pharmedica USA is recalling Purely Soothing 15% MSM Drops because they may not be sterile. This could pose a health risk if the product is used without proper sterility. The recall covers specific bottle sizes and UPC numbers.
Non-sterility means the product could contain harmful bacteria or other contaminants that might cause infections if used internally. This is a health risk, especially for individuals with compromised immune systems or those using the product for medical conditions.
People who own the recalled Purely Soothing 15% MSM Drops bottles with the listed UPCs and lot numbers are affected. Those using the product for medical purposes may be at higher risk due to potential contamination.
Check for bottles labeled 15 ml (0.5 fl oz) or 30 ml (1.014 fl oz) with UPC 7 31034 91382 9 or 7 31034 91379 9. The lot numbers are 1808051 (for 15 ml) and 2203PS01 (for 30 ml).
Identify if your bottle has the listed UPC numbers and lot numbers to confirm it's affected.
The hazard is non-sterility, meaning the product may contain harmful bacteria or contaminants that could cause infections if used internally.
Check for bottles labeled 15 ml (0.5 fl oz) or 30 ml (1.014 fl oz) with UPC 7 31034 91382 9 or 7 31034 91379 9 and lot numbers 1808051 or 2203PS01.
The recall record does not specify a remedy, so contact Pharmedica USA directly for guidance.
We’ve drafted a message you can send Pharmedica to request your refund or repair — edit it as you like.
Subject: Recall D-0456-2023 — Pharmedica Pharmedica Hello, I own a Pharmedica that is covered by recall D-0456-2023 from Pharmedica. 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.
