FDA recall record

Amlodipine besylate and Atorvastatin calcium Tablets,10 mg/40 mg recall — FDA D-1378-2015

Subpotent Drug: Subpotent atorvastatin.

Class IIIclassification
D-1378-2015official record ID
Sep 2, 2015report date

Recall record at a glance

Official recordD-1378-2015
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmDr. Reddy's Laboratories, Inc.
Report dateSep 2, 2015
Recall initiation dateAug 13, 2015
Quantitya) 16,848 and b) 216 Bottles
LocationPrinceton, NJ, United States

Official product description

Amlodipine besylate and Atorvastatin calcium Tablets,10 mg/40 mg, Packaged in a) 30 Count Bottles (NDC: 43598-315-30) and b) 90 Count Bottles (NDC: 43598-315-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India.

Why the product was recalled

Subpotent Drug: Subpotent atorvastatin.

Distribution information

U.S. Nationwide

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.