PlainRecalls
FDA Drug Low Class III Terminated

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.

Reported: August 12, 2015 Initiated: June 23, 2015 #D-1285-2015

Product Description

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.

Reason for Recall

Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.

Details

Units Affected
11,445 Bottles
Distribution
U.S. Nationwide including Puerto Rico.
Location
Davie, FL

Frequently Asked Questions

What product 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.. Recalled by Actavis Laboratories, FL, Inc.. Units affected: 11,445 Bottles.
Why was this product recalled?
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 12, 2015. Severity: Low. Recall number: D-1285-2015.