Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2464-01
Reported: February 12, 2020 Initiated: January 27, 2020 #D-0830-2020
Product Description
Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2464-01
Reason for Recall
GMP Deviations: Product bottle may be absent of desiccant.
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 22,868 bottles
- Distribution
- Nationwide within the United States
- Location
- Parsippany, NJ
Frequently Asked Questions
What product was recalled? ▼
Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2464-01. Recalled by Teva Pharmaceuticals USA. Units affected: 22,868 bottles.
Why was this product recalled? ▼
GMP Deviations: Product bottle may be absent of desiccant.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 12, 2020. Severity: Moderate. Recall number: D-0830-2020.
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