Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging Services Due to Failed Dissolution Specifications. High dissolution results were obtained...
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 Mckesson Packaging Services directly.
Affected Products
Diltiazem HCl Extended-Release Capsules, USP 120 mg, 100-count bottles, Rx only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-014-10
Quantity: 4266 cartons
Why Was This Recalled?
Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mckesson Packaging Services
Mckesson Packaging Services has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report