FDA recall D-0823-2016

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.

Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date

Distribution

Nationwide

Key facts

Status

Terminated

Initiation date

2016-03-31

Report date

2016-04-20

Termination date

2017-01-11

Voluntary/Mandated

Voluntary: Firm initiated

Location

Columbus, OH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0823-2016