CLASS II Drug recall · Reported 12 Dec 2012 · FDA Enforcement Report
Thyro-Tab 088 mg recalled by Lloyd Inc. of Iowa
Lloyd Inc. of Iowa is recalling Thyro-Tab 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
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.
Questions about this recall
Is Thyro-Tab 088 mg recalled?
Yes. Lloyd Inc. of Iowa recalled Thyro-Tab 088 mg on 9 Jul 2012. The recall is Class II and its status is Terminated. Recall number D-076-2013.
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Lloyd Inc. of Iowa
All 36| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Lloyd Thyro-Tab 200 mg recalled by Lloyd Inc. of Iowa | Lloyd Inc. of Iowa | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothroid (levothyroxine sodium tablets, USP), 175 mcg recalled | Lloyd Inc. of Iowa | Potency & Assay | Nationwide |
| Drug | CLASS II | Lloyd Thyro-Tab 175 mg recalled by Lloyd Inc. of Iowa | Lloyd Inc. of Iowa | Potency & Assay | Nationwide |
| Drug | CLASS II | Lloyd Thyro-Tab 137 mg recalled by Lloyd Inc. of Iowa | Lloyd Inc. of Iowa | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothroid (levothyroxine sodium tablets, USP) , 125 mcg recalled | Lloyd Inc. of Iowa | Potency & Assay | Nationwide |