FDA recall record

Amerisource Health Services Fenofibrate Capsules (Micronized), 200 mg , 30-count Unit Dose recall — FDA D-0823-2016

Labeling: Incorrect or Missing Lot and/or Exp Date

Class IIIclassification
D-0823-2016official record ID
Apr 20, 2016report date

Recall record at a glance

Official recordD-0823-2016
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAmerisource Health Services
Report dateApr 20, 2016
Recall initiation dateMar 31, 2016
Quantity5,034 cartons (151,020 capsules)
LocationColumbus, OH, United States

Official product description

Fenofibrate Capsules (Micronized), 200 mg , 30-count Unit Dose Blister Packs per carton, Rx Only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 Carton of 30:NDC 68084-835-32, Individual Dose: NDC 68084-835-33.

Why the product was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date

Distribution information

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.

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