Dr. Berne's Whole Health Products recalls 15% MSM Mist solution bottles due to CGMP deviations. Affected lots expire May 2024 through November 2024. No specific remedy stated in recall.
CGMP Deviations
Dr. Berne's Whole Health Products is recalling their 15% MSM Mist solution bottles because of manufacturing quality control issues. This recall affects specific production lots that expire through November 2024. The issue does not involve immediate safety risks but requires consumers to check their bottles.
CGMP deviations refer to manufacturing quality control failures that could affect product safety and purity. These deviations might mean the product does not meet the required standards for health use, but the recall does not specify immediate health risks.
Owners of Dr. Berne's MSM Mist 15% Solution bottles with lot numbers 6617 through 6716 are affected. People using these products for health purposes may be at risk if they have the recalled lots.
Check the bottle for lot numbers: 6617 (expires May 2024), 6623 (expires June 2024), 6646 (expires July 2024), 6675 (expires September 2024), or 6716 (expires November 2024). The product is a 30 mL/1.014 oz bottle distributed by Dr. Berne's Whole Health Products.
Look for lot numbers on the bottle: 6617, 6623, 6646, 6675, or 6716.
Dr. Berne's Whole Health Products is recalling specific lots of their 15% MSM Mist solution due to manufacturing quality control deviations.
Check the bottle for lot numbers: 6617 (expires May 2024), 6623 (expires June 2024), 6646 (expires July 2024), 6675 (expires September 2024), or 6716 (expires November 2024).
The recall does not specify a remedy, so no action is required beyond checking your product lot number.
We’ve drafted a message you can send Dr. Berne's to request your refund or repair — edit it as you like.
Subject: Recall D-0034-2024 — Dr. Berne's Dr. Berne's Hello, I own a Dr. Berne's that is covered by recall D-0034-2024 from Dr. Berne's. 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.
