Dr. Ergin's SugarMD Advanced Glucose Support Capsules are recalled because they contain unapproved metformin and glyburide. These capsules were sold with specific UPC codes and expiration dates. Consumers should stop using them immediately.
MARKETED WITHOUT AN APPROVED NDA/ANDA: Product found to be tainted with metformin and glyburide
Dr. Ergin's SugarMD Advanced Glucose Support Capsules are being recalled because they were found to contain metformin and glyburide without proper FDA approval. This poses a risk of serious health issues due to the unapproved medications.
The capsules contain metformin and glyburide, which are prescription medications not approved for use in dietary supplements. These drugs can cause serious health risks such as hypoglycemia or other adverse effects when taken without proper medical supervision.
Anyone who purchased Dr. Ergin's SugarMD Advanced Glucose Support Capsules with the listed UPC codes and expiration dates. People with diabetes or those using glucose management supplements are at higher risk.
Check for the following UPC codes: 1 95893 92767 8 (60 count), 1 95893 54697 8 (120 count), or 1 95893 99957 6 (180 count). The capsules were manufactured with expiration date 09/30/2024.
Immediately stop using the recalled capsules as they contain unapproved prescription medications that could cause serious health risks.
The capsules were found to contain metformin and glyburide without FDA approval, which can cause serious health risks.
The recalled capsules have UPC codes: 1 95893 92767 8 (60 count), 1 95893 54697 8 (120 count), and 1 95893 99957 6 (180 count).
The recall record does not specify a return process, so contact the manufacturer directly for instructions.
We’ve drafted a message you can send Dr. Ergin's SugarMD to request your refund or repair — edit it as you like.
Subject: Recall D-0138-2024 — Dr. Ergin's SugarMD Dr. Ergin's SugarMD Hello, I own a Dr. Ergin's SugarMD that is covered by recall D-0138-2024 from Dr. Ergin's SugarMD. 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.
