Delivery Method: VIA Electronic Mail Reference #: 320-26-11 Product: Drugs Over-the-Counter Drugs Recipient: Recipient Name Dr. Donald R. Owen Recipient Title Chief Executive Officer Owen Biosciences, Inc. 7053 Revenue Drive Baton Rouge, LA 70809-4918 …
Delivery Method: VIA Electronic Mail Product: Drugs Recipient: VarunKart Group LLC dba Organic Wellnesses 8206 Louisiana Blvd NE, STE A #4959 Albuquerque, NM 87113 United States support@organicwellnesses.com Issuing Office: Center for Drug Evaluation and …
Delivery Method: Via Email Product: Drugs Recipient: Recipient Name Venkata Vamsi Krishna Kothuri Distacart Inc. 883 N Shoreline Blvd, Suite B220 Mountain View, CA 94043 United States happy@distacart.com Issuing Office: Center for Drug Evaluation and …
Delivery Method: Via Email Product: Drugs Issuing Office: Center for Drug Evaluation and Research (CDER) United States WARNING LETTER November 17, 2025 RE: 716644 Neena Chowdary Koganti: This letter is to advise you that the U.S. Food and Drug …
Delivery Method: Via Email Product: Drugs Recipient: Recipient Name Hiren Gaglani Handelnine Global, LLC dba Navafresh 4300 S. Clinton Ave. South Plainfield, NJ 07080 United States info@navafresh.com Issuing Office: Center for Drug Evaluation and Research …
Delivery Method: Via Email Product: Drugs Issuing Office: Center for Drug Evaluation and Research (CDER) United States WARNING LETTER November 17, 2025 RE: 716286 Mahesh Chada: This letter is to advise you that the U.S. Food and Drug Administration (FDA) …
Delivery Method: Via Electronic Mail - Return Receipt Requested Product: Drugs Recipient: Recipient Name Andrew C. Corbin Wells Pharma of Houston, LLC 9265 Kirby Drive Houston, TX 77054-2520 United States Issuing Office: Center for Drug Evaluation and …
Acclaimed actress and breast cancer survivor Mahima Chaudhary champions proactive women’s health and early detection at the 2025 BCYW Conference DENVER, CO, UNITED STATES, November 25, 2025 /EINPresswire.com/ -- The second International Conference on …
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product Product Name: …
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