The Recall Desk

FDA (Drugs) recall action 73715

Amerisource Health Services recalled 2 products on 2016-04-20

The FDA (Drugs) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2016-04-20
Critical
0
Units
—

Why these products were recalled

Labeling: Incorrect or Missing Lot and/or Exp Date

The agency’s own wording, quoted from the enforcement report.

1–2 of 2

  • LowFDA (Drugs)··2016-04-20

    Amerisource Health Services Recalls Fenofibrate Capsules Due to Labeling Errors

    Amerisource Health Services is recalling 228 cartons of Fenofibrate Capsules because some units have incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized), 134 mg Capsules, 20-count Unit Dose Blister Packs per carton, Rx Only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217, Carton of 20: NDC 68084-835-32, Individual Dose: NDC 68084-835-33.
    Category
    Distribution
    0 states
  • LowFDA (Drugs)··2016-04-20

    Amerisource Recalls Fenofibrate Capsules Due to Incorrect or Missing Labeling

    Amerisource Health Services is recalling 5,034 cartons of Fenofibrate Capsules (Micronized), 200 mg, due to incorrect or missing lot and expiration dates.

    Product
    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.
    Category
    Distribution
    0 states