Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Venlafaxine Hydrochloride Extended-Release Capsules USP Recalled by Lucid Pharma LLC Due to Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lucid Pharma LLC directly.
Affected Products
Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.
Quantity: a) 44168 bottles; b) 24960 bottles
Why Was This Recalled?
Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lucid Pharma LLC
Lucid Pharma LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report