The Recall Desk

FDA (Drugs) recall action 93368

Glenmark Pharmaceuticals Inc., USA recalled 2 products on 2023-12-06

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
2023-12-06
Critical
0
Units
37,200

Why these products were recalled

Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

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

  • HighFDA (Drugs)··2023-12-06

    Prescription Drug Indomethacin Recalled Due to Label Mix-Up

    Glenmark Pharmaceuticals is recalling 37,200 bottles of Indomethacin 25mg capsules distributed nationwide because the bottles may be labeled as Naproxen instead. This labeling error could cause medication confusion.

    Product
    INDOMETHACIN (INDOMETHACIN)
    Category
    Distribution
    0 states