Reported May 29, 2013 · Terminated

Levothroid (levothyroxine sodium tablets, USP), 175 mcg, RX only, 100 tablets per bottle, Manufactured for Forest…

Lloyd Inc. of Iowa

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: Lloyd Inc. of Iowa · 604 W Thomas Ave · Shenandoah, IA · 51601-1744

Is this the product you have?

  • Levothroid (levothyroxine sodium tablets, USP), 175 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1326-01
Lot codes and dates
    • Lot #r: 1095922
    • Exp May-13
    • 1097735
    • Exp Jul-13
    • 1099892
    • Exp Oct-13
Amount recalled
32,345 Bottles

This recall covers 20 products

The agency filed one notice per product. You are reading one of them; the other 19 are below.

7 more are in the archive.

Where it was sold

Why it was recalled

cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.

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 May 8, 2014 · Data as of Sep 19, 6:34 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.