June 2013 FDA Recall Drug by Carefusion 213, Llc
D-1442-2014 - Lack of Assurance of Sterility; Immediate product pouches may not be properly sealed.

This Class II drug recall was voluntarily initiated by Carefusion 213, Llc on June 13, 2013 for the product Drug. The FDA reported the reason for recall as lack of assurance of sterility; immediate product pouches may not be properly sealed.. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-1442-2014

Reason for Recall
Lack of Assurance of Sterility; Immediate product pouches may not be properly sealed.
Initiated
06-13-2013
Reported
07-23-2014
Quantity
23,000 Applicators

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Nationwide in U.S.
ChloraPrep With Tint, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), 26 mL APPLICATOR, Hi-Lite Orange. Rx Only. CareFusion, El Paso, TX 79912. NDC: 054365-400-13.

Batch or Lot Expiration Information

Lot# : 71132, Expiry: 02/2017