Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pantoprazole Sodium Delayed Release Tablets Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due to CGMP Deviation: Presence of dark brown discoloration on...
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 Jubilant Cadista Pharmaceuticals, Inc. directly.
Affected Products
Pantoprazole Sodium Delayed Release Tablets, USP, 40 mg, packaged in 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd, Roorkee - 247661, India, Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-284-90
Quantity: 63,216 bottles
Why Was This Recalled?
CGMP Deviation: Presence of dark brown discoloration on edges of tablets.
Where Was This Sold?
This product was distributed to 4 states: MS, OH, RI, TN
About Jubilant Cadista Pharmaceuticals, Inc.
Jubilant Cadista Pharmaceuticals, Inc. has 29 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report