The Recall Desk

FDA (Drugs) recall action 98790

CareFusion 213, LLC recalled 2 products on 2026-05-13

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
2026-05-13
Critical
0
Units
—

Why these products were recalled

Lack of assurance of Sterility: potential product contamination

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

1–2 of 2

  • SevereFDA (Drugs)··2026-05-13

    PurPrep Povidone-Iodine and Isopropyl Alcohol Solution Recalled for Sterility Assurance

    CareFusion 213, LLC is recalling PurPrep sterile topical solution due to lack of assurance of sterility and potential product contamination. The affected product is a povidone-iodine and isopropyl alcohol solution distributed nationwide.

    Product
    PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
    Category
    Distribution
    0 states
  • SevereFDA (Drugs)··2026-05-13

    BD PurPrep Povidone-Iodine Topical Solution Sterility Assurance Recall

    CareFusion 213, LLC is recalling BD PurPrep (povidone-iodine 8.3% with isopropyl alcohol 72.5%) due to lack of assurance of sterility and potential product contamination. Affected lots are distributed nationwide.

    Product
    PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
    Category
    Distribution
    0 states