CLASS II Drug recall · Reported 4 Jul 2012 · FDA Enforcement Report
Thyro-Tab.075 mg recalled by Lloyd
Lloyd is recalling Thyro-Tab.075 mg, distributed nationwide in the US. The recall was initiated on 24 Feb 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-1395-2012
- FDA event ID
- 61252
- Recalling firm
- Lloyd, Shenandoah, IA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 24 Feb 2012
- FDA classified
- 22 Jun 2012
- Reported
- 4 Jul 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Potency & Assay
Timeline
| 24 Feb 2012 | Recall initiated by company | |
| 22 Jun 2012 | Classified by FDA | +119 days |
| 4 Jul 2012 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.
Product as listed by the FDA
Thyro-Tab.075 mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, Iowa 51601.
Where it was distributed
Nationwide
Questions about this recall
Is Thyro-Tab.075 mg recalled?
Yes. Lloyd recalled Thyro-Tab.075 mg on 24 Feb 2012. The recall is Class II and its status is Terminated. Recall number D-1395-2012.
Why was it recalled?
Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Which lots are affected?
HD17811
Where was it sold?
Nationwide
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
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Levothroid (levothyroxine sodium tablets, USP), 50 mcg recalled by Lloyd | Lloyd | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothroid (levothyroxine sodium tablets, USP), 75 mcg recalled by Lloyd | Lloyd | Potency & Assay | Nationwide |
| Drug | CLASS II | Thyro-Tab 050mg recalled by Lloyd | Lloyd | Potency & Assay | Nationwide |