Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Desmopressin Acetate Tablets Recalled by Actavis Laboratories, FL, Inc. Due to Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly...
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
Desmopressin Acetate Tablets, 0.1mg, 100 Count Bottles, Rx Only. Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA; Distributed by Actavis Pharma, Inc. Parsippany, NJ 07054 USA. NDC: 0591-2464-01.
Quantity: 11,445 Bottles
Why Was This Recalled?
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
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