SugarMDs LLC and the FDA are issuing a nationwide recall of Advanced Glucose Support Supplements after the FDA discovered the presence of undeclared substances in the capsules. Use of the supplement may lead to dangerous health outcomes.
As of the writing of this notice, no reports of adverse events have yet been received.
SUMMARY
Date of Recall:
Announced: November 8, 2023
Public Notification: November 15, 2023
Name(s) of Drug:
SugarMD Advanced Glucose Support, Dietary Supplement
Company Name:
SugarMDs, LLC
Drug Indication:
Glucose Dietary Supplement
Product Description
The supplements were sold online via www.SugarMDs.com and www.amazon.com. Capsules were packaged in 60-count, 120-count, and 180-count bottles with a blue and green label affixed that indicates ADVANCED GLUCOSE SUPPORT.
Reason for Recall
The FDA, during analysis of the supplement, found Glyburide and Metformin. While the drugs are approved for use in the U.S., they are not permitted to be present in dietary supplements. Additionally, the packaging does not indicate the presence of the drugs.
Impacts
Consumers who use the supplement are at a risk of experiencing life-threatening hypoglycemia (low blood sugar), particularly if they are already taking those medications separately.
Symptoms of hypoglycemia (low blood sugar) include:
- Tachycardia (fast heart rate)
- Shaking
- Diaphoresis (sweating)
- Anxiety (nervousness)
- Irritability
- Headache
- Drowsiness
- Hunger
- Seizures
- Coma
- Death
Lot Information
Consumers who use SugarMD Advanced Glucose Support should compare the information on the list below to their supplement package. If the information matches, read further to determine what actions must be taken to participate in the recall.
Product |
UPC # |
LOT # |
Expiration Date |
SugarMD Advanced Glucose Support Dietary Supplement, 60-Count Bottle | 00195893927678 | 22165-003 | 09/2024 |
SugarMD Advanced Glucose Support Dietary Supplement, 120-Count Bottle | 00195893546978 | 22165-003 | 09/2024 |
SugarMD Advanced Glucose Support Dietary Supplement, 180 Count Bottle | 00195893999576 | 22165-003 | 09/2024 |
Have you found that your medication is part of the recall? Here’s what you should do:
Consumers
- Call your doctor right away. Report the use of the recalled medication.
- Monitor your health for any adverse symptoms and notify your physician if any concerns are noted.
- Consumers with questions may contact SugarMDs LLC at (561) 462-5053. They are available Monday-Friday from 9 a.m. to 5 p.m. EST. They can also be reached via email at feedback@sugarmds.com.
- If you are currently experiencing or have experienced an adverse reaction to this medication (listed above), notify your physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
- Contact MedWaste Management for information and assistance with disposing of the recalled medication.
Retailer
- Examine all inventory and remove stock affected by the recall immediately.
- Contact SugarMDs LLC at (561) 462-5053. They are available Monday-Friday from 9 a.m. to 5 p.m. EST. They can also be reached via email at feedback@sugarmds.com. Notify them of any recalled batches that have already been sold to consumers.
- Notify affected consumers of recalled batches that they have already or will receive.
- Contact MedWaste Management for information and assistance with disposing of the recalled medication.
Wholesaler
- Examine all inventory and remove stock affected by the recall immediately.
- Contact SugarMDs LLC at (561) 462-5053. They are available Monday-Friday from 9 a.m. to 5 p.m. EST. They can also be reached via email at feedback@sugarmds.com. Notify them of any recalled batches that have already been shipped to retailers.
- Notify affected retailers of recalled batches that they have already or will receive.
- Contact MedWaste Management for information and assistance with disposing of the recalled medication.
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