FDA recall record

CareFusion 213 ChloraPrep With Tint, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v recall — FDA D-1442-2014

Lack of Assurance of Sterility; Immediate product pouches may not be properly sealed.

Class IIclassification
D-1442-2014official record ID
Jul 23, 2014report date

Recall record at a glance

Official recordD-1442-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCareFusion 213, LLC
Report dateJul 23, 2014
Recall initiation dateJun 13, 2013
Quantity23,000 Applicators
LocationEl Paso, TX, United States

Official product description

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.

Why the product was recalled

Lack of Assurance of Sterility; Immediate product pouches may not be properly sealed.

Distribution information

Nationwide in U.S.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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