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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 61252

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 24, 2012
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Lloyd Inc

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 2

Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, Iowa 51601

D-1394-2012
Recall number
D-1394-2012
Initiated
February 24, 2012
Classification
Class II
Status
Terminated
Recalling firm
Lloyd Inc
Quantity
19,039 bottles

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Subpotent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

Code information

LOT NO.1092045

Distribution pattern

Nationwide

drug · product 2 of 2

Thyro-Tab.075 mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, Iowa 51601.

D-1395-2012
Recall number
D-1395-2012
Initiated
February 24, 2012
Classification
Class II
Status
Terminated
Recalling firm
Lloyd Inc
Quantity
1,913,236 tablets

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Subpotent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

Code information

HD17811

Distribution pattern

Nationwide