Data Foundry

Drug recalls 2026

BD ChloraPrep Scrub Teal — Class II drug recall D-0649-2026

Ongoing recall by CareFusion 213, LLC, reported 2026-07-08, distributed nationwide. Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing

Recall numberD-0649-2026
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmCareFusion 213, LLC, El Paso, TX, United States
Recall initiated2026-06-11
Classified2026-06-29
Reported by FDA2026-07-08
DistributedNationwide (US)
Quantity1,200 units
Reason classessterility
NDC54365-0400, 54365-0400-36
Model numbers930725NS, 930725NSB
Expiration dates2026-10-31, 2026-12-31, 2027-01-31, 2027-04-30, 2027-05-31, 2027-09-30, 2027-12-31, 2028-03-31, 2028-04-30

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.

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0649-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.