US Drug Recall Register
Class II · Moderate risk Terminated 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.

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