The Recall Desk

FDA (Drugs) recall action 61252

Lloyd Inc recalled 2 products on 2012-07-04

The FDA (Drugs) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2012-07-04
Critical
0
Units
1,932,275

Why these products were recalled

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

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

1–2 of 2

  • ModerateFDA (Drugs)··2012-07-04

    Lloyd Inc Recalls Subpotent Levothroid Levothyroxine Sodium Tablets

    Lloyd Inc is recalling 19,039 bottles of Levothroid 75 mcg tablets because the drug tested below the required potency level.

    Product
    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
    Category
    Distribution
    0 states
  • SevereFDA (Drugs)··2012-07-04

    Lloyd Inc Recalls Subpotent Thyro-Tab 0.75 mg Tablets

    Lloyd Inc is recalling 1,913,236 Thyro-Tab 0.75 mg tablets because they failed potency testing at the 6-month interval.

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