CLASS II Drug recall · Reported 12 Dec 2012 · FDA Enforcement Report

Thyro-Tab 0.088 mg recalled by Lloyd Inc. of Iowa

Lloyd Inc. of Iowa is recalling Thyro-Tab 0.088 mg, distributed nationwide in the US. The recall was initiated on 9 Jul 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #HA31411 and #HE17811

Quantity recalled3,826,269 tablets

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number: D-076-2013
FDA event ID: 62511
Recalling firm: Lloyd Inc. of Iowa, Shenandoah, IA
Classification: Class II
Status: Terminated
Recall initiated: 9 Jul 2012
FDA classified: 3 Dec 2012
Reported: 12 Dec 2012
Type: Voluntary: Firm initiated
Customers notified by: Telephone
Reason category: Manufacturing (CGMP) Deviations

Timeline

9 Jul 2012	Recall initiated by company
3 Dec 2012	Classified by FDA	+147 days
12 Dec 2012	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

cGMP Deviations; does not meet in process specification requirements

Product as listed by the FDA

Thyro-Tab 0.088 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Where it was distributed

Distribution was nationwide, including Puerto Rico. There was no foreign, military, or government distribution.

Nationwide Puerto Rico

Questions about this recall

Why was it recalled?

cGMP Deviations; does not meet in process specification requirements

Which lots are affected?

Lot #HA31411 and #HE17811

Where was it sold?

Distribution was nationwide, including Puerto Rico. There was no foreign, military, or government distribution.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

11 other products · FDA event 62511

This product is part of a recall event; the main page for the event is Levothroid (levothyroxine sodium tablets, USP), 112 mcg recalled.

Reported	Class	Recall	Company	Reason	Where
12 Dec 2012	CLASS II	Levothroid (levothyroxine sodium tablets, USP), 112 mcg recalled	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Levothroid (levothyroxine sodium tablets, USP), 137 mcg recalled	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Thyro-Tab 0.137 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Levothroid (levothyroxine sodium tablets, USP),125 mcg recalled	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Levothroid (levothyroxine sodium tablets, USP), 88 mcg recalled	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Thyro-Tab 0.050 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Levothroid (levothyroxine sodium tablets, USP), 300 mcg recalled	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Thyro-Tab 0.112 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Levothroid (levothyroxine sodium tablets, USP), 50 mcg recalled	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Thyro-Tab 0.125 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012	CLASS II	Thyro-Tab 0.300 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide

More recalls from Lloyd Inc. of Iowa

All 36

Reported	Class	Recall	Company	Reason	Where
29 May 2013Drug	CLASS II	Lloyd Thyro-Tab 0.200 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Potency & Assay	Nationwide
29 May 2013Drug	CLASS II	Levothroid (levothyroxine sodium tablets, USP), 175 mcg recalled	Lloyd Inc. of Iowa	Potency & Assay	Nationwide
29 May 2013Drug	CLASS II	Lloyd Thyro-Tab 0.175 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Potency & Assay	Nationwide
29 May 2013Drug	CLASS II	Lloyd Thyro-Tab 0.137 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Potency & Assay	Nationwide
29 May 2013Drug	CLASS II	Levothroid (levothyroxine sodium tablets, USP) , 125 mcg recalled	Lloyd Inc. of Iowa	Potency & Assay	Nationwide

Other Thyro-tab recalls

All 10

Reported	Class	Recall	Company	Reason	Where
2 Jan 2013Drug	CLASS II	Thyro-Tab 0.050 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Potency & Assay	Nationwide
2 Jan 2013Drug	CLASS II	Thyro-Tab 0.075 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Potency & Assay	Nationwide
12 Dec 2012Drug	CLASS II	Thyro-Tab 0.300 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012Drug	CLASS II	Thyro-Tab 0.125 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide
12 Dec 2012Drug	CLASS II	Thyro-Tab 0.112 mg recalled by Lloyd Inc. of Iowa	Lloyd Inc. of Iowa	Manufacturing (CGMP) Deviations	Nationwide