Reported Apr 20, 2016 · Terminated

Fenofibrate Capsules (Micronized), 200 mg , 30-count Unit Dose Blister Packs per carton, Rx Only, Packaged and…

Amerisource Health Services

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Amerisource Health Services · 2550 John Glenn Ave · Columbus, OH · 43217-1188

Is this the product you have?

  • Fenofibrate Capsules (Micronized), 200 mg , 30-count Unit Dose Blister Packs per carton, Rx Only
  • Packaged and Distributed byAmerican Health Packaging Columbus
  • Ohio 43217 Carton of 30NDC 68084-835-32
  • Individual DoseNDC 68084-835-33
Lot codes and dates
    • Lot #142548
    • Exp. 05/16 Lot #145036
    • Exp. 10/16 Lot #151170
    • Exp. 03/17 Lot #152978
    • Exp. 09/17 Lot #155080
    • Exp. 01/18
Amount recalled
5,034 cartons (151,020 capsules)

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jan 11, 2017 · Data as of Sep 19, 6:25 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.