The Recall Desk

FDA (Drugs) recall action 61094

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
1,943,463

Why these products were recalled

Subpotent (Single Ingredient Drug): Low assay at the 9-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 19,166 bottles of Levothroid 50 mcg tablets because they failed potency testing at 9 months.

    Product
    Levothroid (levothyroxine sodium tablets, USP), 50 mcg., packaged in 100-ct. bottles, RX, NDC 0456-1321-01. Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.
    Category
    Distribution
    0 states
  • ModerateFDA (Drugs)··2012-07-04

    Lloyd Inc Recalls Subpotent Thyro-Tab 0.050mg Bulk Tablets

    Lloyd Inc is recalling 1,924,297 bulk Thyro-Tab 0.050mg tablets because they failed potency testing at the 9-month interval. The product was distributed nationwide and to Puerto Rico.

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