The Food and Drug Administration is advising consumers not to purchase or use X3 500K GOLD EDITION, a product promoted and sold for sexual enhancement on various websites and possibly in some retail stores.
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Medication Health Fraud for Specific Diseases and Conditions
FDA has identified condition-specific medication health fraud scams that can pose significant risks to consumers.Fusion IV Pharmaceuticals Inc. dba Axia Pharmaceuticals, Los Angeles, CA. Amended 483 Issued 03/23/2017
Fusion IV Pharmaceuticals Inc. dba Axia Pharmaceuticals, Los Angeles, CA. Amended 483 Issued 03/23/2017Task Description Request Please post to the 2017 Pharmacy Inspections and Related Records Web page
Record Date 03/23/2017
FEI Number 3013341563
Firm Name Fusion IV Pharmaceuticals Inc. dba Axia PDrug Trials Snapshots: VIZZ
Drug Trials Snapshots: VIZZResource Capacity Planning and Modernized Time Reporting
FDA is making optimal use of its financial resources to maximize its ability to efficiently and effectively deliver on its commitments to the public.W.W. Industrial Group Recalls Pear Slices in Juice Due to Elevated Levels of Lead and Cadmium
W.W. Industrial Group, Inc., NY is recalling Parashore Pear Slices in juice, 15 oz, because they have the potential to be contaminated with elevated levels of lead and cadmium.Dr. Reddy’s Laboratories, Mirfield, West Yorkshire, UK 9.1-9.5.25_483
Record Date: 09/05/2025
Entity Name: Dr. Reddy’s Laboratories (EU) Ltd.
FEI Number: 3002807544
Record Type: 483
Country: United Kingdom
Establishment Type: API Manufacturer