SUGARMDS LLC recalls Dr. Ergin's SugarMD, ADVANCED GLUCOSE SUPPORT Capsules, Dietary Supplement, helps support healthy glucose levels a) 60 count (UPC 1 95893…
MARKETED WITHOUT AN APPROVED NDA/ANDA: Product found to be tainted with metformin and glyburide
Read the official notice →- Date
- 2023-12-13
- Country
- United States
- Brand
- SUGARMDS LLC
- Product
- Dr. Ergin's SugarMD, ADVANCED GLUCOSE SUPPORT Capsules, Dietary Supplement, helps support healthy glucose levels a) 60 count (UPC 1 95893…
- Classification
- Class I
- Units
- U.S. Nationwide and online websites.
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
Other drugs & medical recalls in the United States
- 2023-12-13
US
US
Right Value Drug Stores, LLC dba Carie Boyd's Prescription… recalls LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel), Single-use…
Product Mix-up: Incorrect Product Formulation
FDA · DrugRight Value Drug Stores, LLC dba Carie Boyd's Prescription…USA NationwideOfficial notice →US
Padagis US LLC recalls Trospium Chloride Extended-Release Capsules, 60 mg, 30 Capsules per bottle, Rx Only, Manufactured By: Sidmak Laboratories (India) Pvt.…
Failed Tablets/Capsules specifications; missing/broken/extra tablets within the capsules
US
- 2023-12-06
US
Siemens Healthcare Diagnostics Inc recalls RAPIDPOINT 500 Blood Gas System
There are potential drug interferences from Perhexiline Maleate or Atomoxetine Hydrochloride that may cause falsely elevated sodium results reported on the RAPIDPoint 500 and RAPIDPoint 500e Blood Gas Systems. The…
FDA · DeviceSiemens Healthcare Diagnostics IncDomestic: Nationwide Distribution. Foreign: Albania, Algeria, Angola,…Official notice →US
Medtronic Inc. recalls ICM LNQ22 LINQ II, Model LNQ22; Insertable Cardiac Monitor
It may create the potential for amplified noise and/or overall signal reduction of the ICM, which may interfere with intended recordings of heart rhythms. This noise pattern is different from occasional noise due to…
FDA · DeviceMedtronic Inc.US and Australia, Austria, Belgium, Brunei Darussalam, Canada, Czech Republic,…Official notice →