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

Medline Suture Removal Tray, Sterile, Single Use Only. Packaged in USA 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 Suture Removal Tray, Sterile, Single Use Only. Packaged in USA 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-0285-2018

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.