FDA recall record

Dofetilide Capsules 500 mcg (0.5mg), 60-count bottle recall — FDA D-1082-2023

Out of Specification result observed in content uniformity testing

Class IIIclassification
D-1082-2023official record ID
Aug 16, 2023report date

Recall record at a glance

Official recordD-1082-2023
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmSUN PHARMACEUTICAL INDUSTRIES Inc.
Report dateAug 16, 2023
Recall initiation dateJul 18, 2023
Quantity360 60-count bottles
LocationPrinceton, NJ, United States

Official product description

Dofetilide Capsules 500 mcg (0.5mg), 60-count bottle, Rx Only, Manufactured by Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 191, (U.T of D & NH), India, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512. NDC 47335-063-86

Why the product was recalled

Out of Specification result observed in content uniformity testing

Distribution information

Nationwide in the USA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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Class IIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES INC