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Class IIOngoing

BD ChloraPrep Scrub Teal recall

FDA recall D-0649-2026 · initiated Jun 11, 2026

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

CareFusion 213, LLC recalled BD ChloraPrep Scrub Teal in Jun 2026 — an FDA Class II recall (D-0649-2026) 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
BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 100 x 10.5 mL Applicators/case, NDC 54365-400-36, catalog number 930725NS; b) 100 x 10.5 mL Applicators/case, bulk catalog number 930725NSB; STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co.
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 BD ChloraPrep Scrub Teal recalled?
CareFusion 213, LLC recalled BD ChloraPrep Scrub Teal in Jun 2026 — an FDA Class II recall (D-0649-2026) 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 BD ChloraPrep Scrub Teal recalled?
Per the FDA enforcement record, the reason for recall D-0649-2026 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 BD ChloraPrep Scrub Teal 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 BD ChloraPrep Scrub Teal 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-0649-2026, initiated Jun 2026.

Source: openFDA Drug Enforcement record D-0649-2026

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