FDA recall record

Teva Pharmaceuticals USA Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle recall — FDA D-0830-2020

GMP Deviations: Product bottle may be absent of desiccant.

Class IIclassification
D-0830-2020official record ID
Feb 12, 2020report date

Recall record at a glance

Official recordD-0830-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTeva Pharmaceuticals USA
Report dateFeb 12, 2020
Recall initiation dateJan 27, 2020
Quantity22,868 bottles
LocationParsippany, NJ, United States

Official 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

Why the product was recalled

GMP Deviations: Product bottle may be absent of desiccant.

Distribution information

Nationwide within the United States

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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