Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals Inc. Due to Failed Impurities/Degradation Specifications: Out of specification test results...
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 Mylan Pharmaceuticals Inc. directly.
Affected Products
Diltiazem HCl Extended-Release Capsules, USP 120 mg 500-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505. NDC 0378-5220-05
Quantity: 656 500-count bottles
Why Was This Recalled?
Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mylan Pharmaceuticals Inc.
Mylan Pharmaceuticals Inc. has 71 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report