New Drug/Misbranded
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CelestaPro – 718613 – 11/03/2025
Unapproved New Drugs/Misbranded BotoxUpdated Company Announcement to August 28, 2025, Recall Announcement
Costa Mesa, California — February 13, 2026 — Green Lumber Holding, LLC (“Green Lumber”) is issuing an updated consumer alert regarding counterfeit products falsely marketed as genuine Green Lumber products that may pose potential health risks.StuffbyNainax LLC Issues Voluntary Nationwide Recall of MR.7 SUPER 700000 Dietary Supplement Due to the Presence of Undeclared Sildenafil and Tadalafil
Huntsville, Texas — StuffbyNainax LLC is voluntarily recalling all lots of MR.7 SUPER 700000 capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil and tadalafil, which are active ingredients in FDA-approved prescription drugs used to treat male erectile dysFDA | NIH : Regulatory Do’s and Don’ts: Tips from FDA – 09/04/2024
FDA | NIH : Regulatory Do’s and Don’ts: Tips from FDAOver-The-Counter Monograph Drug User Fee Program (OMUFA)
A user fee program for nonprescription (over-the-counter or OTC) monograph drugs would be a potential funding mechanism to supplement congressional non user-fee appropriations.Early Alert: Dialysis Tubing Set Issue from Vantive
Prismaflex Set deaeration chambers may dislodge from the Prismaflex Control Unit during use.
