Reported Mar 22, 2017 · Terminated

GlipiZIDE Extended-release tablets, 2.5 mg, 30-count carton (NDC 68084-295-21), Individual dose (NDC 68084-395-11), Rx…

Amerisource Health Services

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

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 Ste A · Columbus, OH · 43217-1188

Is this the product you have?

  • GlipiZIDE Extended-release tablets, 2.5 mg, 30-count carton (NDC 68084-295-21), Individual dose (NDC 68084-395-11), Rx Only, Packaged and Distributed by American Health Packaging, Columbus, Ohio 43217, NDC 68084-295-21
Lot codes and dates
    • Lot #160133
    • 160549 Exp. 08/17 Lot #162006
    • Exp. 09/17 Lot #163348A
    • 163348B
    • Exp. 10/17
Amount recalled
19,393 cartons (581,790 extended release tablets)

Where it was sold

  • Nationwide

Why it was recalled

Failed dissolution specifications: Glipizide 2.5 mg ER Tablets exceeded dissolution specification rates for the 10 hour testing point.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

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

Read the FDA (openFDA drug enforcement) notice

Notice updated Mar 1, 2018 · Data as of Sep 19, 7:53 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.