Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Ramipril Capsules Recalled by Actavis Laboratories, FL, Inc. Due to Labeling: Incorrect or Missing Lot And/or Exp Date:...
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 Actavis Laboratories, FL, Inc. directly.
Affected Products
Ramipril Capsules, USP, 1.25 mg, 30-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia, BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 16252-570-30.
Quantity: 15,984 bottles
Why Was This Recalled?
Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the incorrect expiration date of 03/18 rather than 09/17.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Actavis Laboratories, FL, Inc.
Actavis Laboratories, FL, Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report