US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 21, 2017 (9 years ago)

Medline I&D Tray Kit, Sterile, Single use only. Packaged in Mexico for Medline…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

What was recalled

Medline I&D Tray Kit, Sterile, Single use only. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060

Recalling firm
Medline Industries Inc
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0268-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.