The Recall Desk

FDA (Drugs) recall action 82538

Lohxa LLC recalled 2 products on 2019-04-17

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
2019-04-17
Critical
0
Units
—

Why these products were recalled

Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an incorrect Exp Date.

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

States named across these recalls

1–2 of 2

  • ModerateFDA (Drugs)··2019-04-17

    Lohxa Recalls Bismuth Subsalicylate Suspension Due to Incorrect Expiration Date

    Lohxa LLC is recalling Bismuth Subsalicylate Oral Suspension because the labels contain incorrect expiration dates. The affected product was distributed in Massachusetts, New York, and Wyoming.

    Product
    Bismuth Subsalicylate Oral Suspension 262mg/15mL, unit dose cups, OTC, Rpkg. By.: Lohxa Worcester, MA, NDC 70166-059-01
    Category
    Distribution
    3 states
  • ModerateFDA (Drugs)··2019-04-17

    Lohxa Recalls Phenobarbital Oral Solution Due to Incorrect Expiration Date

    Lohxa LLC is recalling Phenobarbital Oral Solution because the labels contain incorrect expiration dates. The affected product was distributed in Massachusetts, New York, and Wyoming.

    Product
    Phenobarbital Oral Solution, USP 20 mg/5mL, unit dose cup, Rx Only, Rpkg. By.Lohxa Worcester, MA 01608 NDC 70166-536-02
    Category
    Distribution
    3 states