Actavis Laboratories, FL, Inc. recalls Desmopressin Acetate Tablets, 0.1mg, 100 Count Bottles, Rx Only. Manufactured by: Actavis Laboratories FL, Inc., Fort L…
- Recall date
- June 23, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1285-2015
- FDA classification
- Class III
- Brand / firm
- Actavis Laboratories, FL, Inc.
- Sold / distributed
- U.S. Nationwide including Puerto Rico.
Why it was recalled
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
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.
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