Carefusion 213, Llc recalls ChloraPrep with Tint, HI-Lite Orange, 3 mL Applicator, Patient Preoperative Skin Preparation, External Use Only, Sterile
Recalled September 26, 2012 · FDA recall D-1674-2012 · Carefusion 213
Hazard
Lack of Assurance of Sterility: A customer complaint reported some units had incomplete seals (open seals) on the Individual unit packaging. · FDA Class II
Units
67,775 Applicators
Sold at
Nationwide
Description
Lack of Assurance of Sterility: A customer complaint reported some units had incomplete seals (open seals) on the Individual unit packaging.
Product
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
Manufacturer(s)
Carefusion 213, Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →