Amerisource Health Services recalls Fenofibrate Capsules (Micronized), 134 mg Capsules, 20-count Unit Dose Blister Packs per carton, Rx Only, Packaged and…
- Recall date
- March 31, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0822-2016
- FDA classification
- Class III
- Brand / firm
- Amerisource Health Services
- Sold / distributed
- Nationwide
Why it was recalled
Labeling: Incorrect or Missing Lot and/or Exp Date
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
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.
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