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Class IIOngoing

ChloraPrep FREPP recall

FDA recall D-0646-2026 · initiated Jun 11, 2026

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Jul 8, 2026How we research

CareFusion 213, LLC recalled ChloraPrep FREPP in Jun 2026 — an FDA Class II recall (D-0646-2026) because Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Details

Product
ChloraPrep FREPP, Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) 500 x 1.5 mL applicators/case, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-30, Catalog number 930599NSB
Recalling company
CareFusion 213, LLC
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Distributed Nationwide in the USA
Initiated
Jun 11, 2026
FDA report date
Jul 8, 2026

This recall is linked to a product we cover: Chloraprep with Tint

What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was ChloraPrep FREPP recalled?
CareFusion 213, LLC recalled ChloraPrep FREPP in Jun 2026 — an FDA Class II recall (D-0646-2026) because Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel. May cause temporary or medically reversible harm; low probability of serious harm.
Why was ChloraPrep FREPP recalled?
Per the FDA enforcement record, the reason for recall D-0646-2026 was: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
Is a recalled ChloraPrep FREPP dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of ChloraPrep FREPP are affected?
Distribution: Distributed Nationwide in the USA. The affected lot numbers and expiration dates are listed in the official FDA enforcement record for recall D-0646-2026, initiated Jun 2026.

Source: openFDA Drug Enforcement record D-0646-2026

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