Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Absorica (isotretinoin) Capsules Recalled by Ranbaxy Inc. Due to Undeclared Excipients
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 Ranbaxy Inc. directly.
Affected Products
Absorica (isotretinoin) Capsules, 25 mg, Packaged in 3 x 10 Count Blister Cards/Box, Rx Only. Manufactured for: RANBAXY LABORATORIES, INC Jacksonville, FL 32257 USA. NDC: 10631-133-31.
Quantity: 9,229 Boxes
Why Was This Recalled?
Incorrect/Undeclared Excipients: Product contains undeclared FD&C Yellow No. 5 in the capsule shell.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ranbaxy Inc.
Ranbaxy Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report