FDAClass I · Drug · Recalled July 1, 2026

BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (I recall — CareFusion 213, LLC

Hazard: Non-Sterility: Due to presence of Aspergillus penicillioides.

Class I: most serious — reasonable probability of serious health consequences or death.

View the official FDA enforcement record (openFDA) ↗

Official recall ID: D-0624-2026
Brand: CareFusion 213
Classification: Class I
Units affected: 193,440 applicators
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), 1 mL Applicator, 60 Applicators per inner Carton, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of Beckton, Dickinson and Co., NDC 54365-400-31.

Affected products

BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (I

Companies & origin

Recalling firm location: El Paso, TX, United States
Firm address: 1550 Northwestern Dr, N/A, 79912-8000

Identifying details (verbatim from the notice)

Product codes / lots: Lot # 4032183, Exp 01/31/2027
Distribution: Nationwide inthe USA, as well as other foreign distribution.
Firm notified the public via: Letter
FDA event ID: 99114
Recall initiated: May 28, 2026
FDA classified: June 25, 2026
FDA report date: July 1, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 24, 2026 at 12:00 AM UTC.

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