Class II · Moderate riskTerminated Initiated Nov 8, 2011 (15 years ago)
ChloraPrep with Tint, HI-Lite Orange, 3 mL Applicator, Patient Preoperative Skin…
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility: A customer complaint reported some units had incomplete seals (open seals) on the Individual unit packaging.
What was recalled
ChloraPrep with Tint, HI-Lite Orange, 3 mL Applicator, Patient Preoperative Skin Preparation, External Use Only, Sterile, product code 260415, Carefusion, Leawood, KS 66211, USA
Recalling firm
Carefusion 213, Llc
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1674-2012
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.