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.
FDA recall notice · announced April 20, 2016 · Amerisource Health Services
Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.
The 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.
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date
Notes
Distribution: Nationwide
Lot/code information: Lot #144332C; Exp. 04/16 Lot #155224; Exp. 05/17
Quantity: 228 cartons ( 4,560 capsules)
Status: Terminated
Products in this recall event:
- 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 (D-0823-2016)
- 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 (D-0822-2016)
Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.