Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Venlafaxine Extended-Release Tablets Recalled by Appco Pharma LLC Due to Failed Tablet/Capsule Specifications: Missing tab ID on either...
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 Appco Pharma LLC directly.
Affected Products
Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.
Quantity: 1380 bottles
Why Was This Recalled?
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Appco Pharma LLC
Appco Pharma LLC has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report