Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ropinirole Recalled by Sandoz, Inc Due to Cross contamination with other products: Sandoz is recalling...
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 Sandoz, Inc directly.
Affected Products
Ropinirole, extended-release tablets, 2 mg, 90 count bottle, Rx only, Manufactured in India by Sandoz Private Ltd, for Sandoz Inc, Princeton, NJ 08540, NDC 0781-5780-92
Quantity: 692 bottles (90 count)
Why Was This Recalled?
Cross contamination with other products: Sandoz is recalling certain lots of Ropinirole Extended Release Tablets 2 mg due to the potential presence of carryover coming from the previously manufactured product, mycophenolate mofetil.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Sandoz, Inc
Sandoz, Inc has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report