Reported May 29, 2013 · Terminated

Levothroid (levothyroxine sodium tablets, USP) , 75 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) , 75 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1322-01
Lot codes and dates
    • Lot #: 1098752
    • Exp. Mar-13
    • 1099890
    • Exp Apr-13
Amount recalled
19,787 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, 5:04 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.