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.
Reported: April 20, 2016 Initiated: March 31, 2016 #D-0822-2016
Product Description
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
Details
- Recalling Firm
- Amerisource Health Services
- Units Affected
- 228 cartons ( 4,560 capsules)
- Distribution
- Nationwide
- Location
- Columbus, OH
Frequently Asked Questions
What product 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.. Recalled by Amerisource Health Services. Units affected: 228 cartons ( 4,560 capsules).
Why was this product recalled? ▼
Labeling: Incorrect or Missing Lot and/or Exp Date
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 20, 2016. Severity: Low. Recall number: D-0822-2016.
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