CLASS I Drug recall · Reported 5 May 2021 · FDA Enforcement Report

BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate recalled

CareFusion 213 is recalling BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol, distributed nationwide in the US. The recall was initiated on 19 Mar 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot and Exp Date: 0065386, 2/28/2023; 0085419, 3/31/2023; 0091666, 3/31/2023; 0149328, 4/30/2023; 0151977, 5/31/2023; 0161217, 5/31/2023; 0175874, 6/30/2023; 0176660, 6/30/2023; 0188805, 6/30/2023; 0211068, 7/31/2023;
NDC54365-400
Quantity recalled952,100 cartons

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0343-2021
FDA event ID
87592
Recalling firm
CareFusion 213, El Paso, TX
Manufacturer
CareFusion 213, LLC
Classification
Class I
Status
Terminated
Recall initiated
19 Mar 2021
FDA classified
26 Apr 2021
Reported
5 May 2021
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Sterility

Timeline

19 Mar 2021Recall initiated by company
26 Apr 2021Classified by FDA+38 days
5 May 2021Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Non-sterility.Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, growth of Aspergillus penicillioides, a type of fungus, resulted in a breach of the package integrity.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Sterile Solution, 0.10 fl. oz. (3 ml) each, 25 Applicators in carton, applicator is sterile if package is intact. CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co, NDC 54365-400-32 REF 930400

Where it was distributed

Distributed Nationwide in the USA and to Singapore, Chile, Oman, Columbia, United Arab Emirates, South Africa, Kuwait, Democratic Republic of the Congo, Qatar, Bahrain, Hong Kong, Brazil.

Nationwide

Questions about this recall

Is BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol recalled?

Yes. CareFusion 213 recalled BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol on 19 Mar 2021. The recall is Class I and its status is Terminated. Recall number D-0343-2021.

Why was it recalled?

Non-sterility.Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, growth of Aspergillus penicillioides, a type of fungus, resulted in a breach of the package integrity.

Which lots are affected?

Lot and Exp Date: 0065386, 2/28/2023; 0085419, 3/31/2023; 0091666, 3/31/2023; 0149328, 4/30/2023; 0151977, 5/31/2023; 0161217, 5/31/2023; 0175874, 6/30/2023; 0176660, 6/30/2023; 0188805, 6/30/2023; 0211068, 7/31/2023;

Where was it sold?

Distributed Nationwide in the USA and to Singapore, Chile, Oman, Columbia, United Arab Emirates, South Africa, Kuwait, Democratic Republic of the Congo, Qatar, Bahrain, Hong Kong, Brazil.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from CareFusion 213

All 48
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIBD ChloraPrep Clear, (2% w/v chlorhexidine gluconate recalledChloraprep One-stepCareFusion 213SterilityNationwide
DrugCLASS IIBD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) recalledChloraprep One-stepCareFusion 213SterilityNationwide
DrugCLASS IIBD ChloraPrep Hi-Lite Orange recalled by CareFusion 213Chloraprep One-stepCareFusion 213SterilityNationwide
DrugCLASS IIBD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate recalledChloraprep One-stepCareFusion 213SterilityNationwide
DrugCLASS IIBD ChloraPrep Hi-Lite Orange recalled by CareFusion 213Chloraprep One-stepCareFusion 213SterilityNationwide

Other Chlorhexidine Gluconate recalls

All 36
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIBD ChloraPrep Clear, (2% w/v chlorhexidine gluconate recalledChloraprep One-stepCareFusion 213SterilityNationwide
DrugCLASS IIBD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) recalledChloraprep One-stepCareFusion 213SterilityNationwide
DrugCLASS IIBD ChloraPrep Hi-Lite Orange recalled by CareFusion 213Chloraprep One-stepCareFusion 213SterilityNationwide
DrugCLASS IIBD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate recalledChloraprep One-stepCareFusion 213SterilityNationwide
DrugCLASS IIBD ChloraPrep Hi-Lite Orange recalled by CareFusion 213Chloraprep One-stepCareFusion 213SterilityNationwide