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Class II: temporary or reversible health riskTerminated

Lloyd Thyro-Tab 0 Recall

Thyro-Tab 0

Lloyd Inc · Shenandoah, IA

Risk level
Class II
Reported by FDA
Jul 4, 2012
Recall ID
D-1392-2012
Check your lot numberHow we source this data

Summary

Lloyd recalled Thyro-Tab 0 starting Feb 3, 2012. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1392-2012 on Jul 4, 2012. Reason: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval. Status: Terminated.

Why it was recalled

Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.

Product description

Thyro-Tab 0.050mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Lot numbers, UPCs & expiration codes

Lot HB06311

Where it was sold

Nationwide and PR.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1392-2012
Classification
Class II
Status
Terminated
Recall initiated
Feb 3, 2012
FDA report date
Jul 4, 2012
Quantity
1,924,297 bulk tablets
Recall type
Voluntary: Firm initiated
Recalling firm
Lloyd Inc

Original FDA data

Every field from FDA enforcement report D-1392-2012, exactly as published.

Show all FDA fields
City
Shenandoah
State
IA
Status
Terminated
Country
United States
Event ID
61094
Address
604 W Thomas Ave
Address (line 2)
Po Box 130
Code information
Lot HB06311
Postal code
51601-1744
Report date
Jul 4, 2012
Product type
Drugs
Recall number
D-1392-2012
Classification
Class II
Recalling firm
Lloyd Inc
Product quantity
1,924,297 bulk tablets
Termination date
Jul 30, 2013
Reason for recall
Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Thyro-Tab 0.050mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.
Distribution pattern
Nationwide and PR.
Recall initiation date
Feb 3, 2012
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jun 22, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1392-2012, published Jul 4, 2012. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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