FDA-Drug2026-07-08Class IIPROCESSING DEFECT
BD ChloraPrep Scrub Teal recalled for lack of sterility assurance
What this means
BD ChloraPrep Scrub Teal applicators intended for further processing and sterilization were mistakenly distributed as finished sterile products. The affected applicators may not meet sterility standards required for safe use in medical settings.
- Check if you have ChloraPrep Scrub Teal lot numbers 3352149 (exp. 12/31/2026), 5028798 (exp. 01/31/2028), or 5069651 (exp. 03/31/2028).
- Do not use applicators from these lots.
- Contact BD customer service or your supplier for instructions on returns or replacements.
The agency's original wording
Hazard
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
Intended for
Adults
Illnesses reported
None reported
Sold states
Distributed Nationwide in the USA
Affected count
125 units
Manufactured in
1550 Northwestern Dr, N/A, El Paso, TX, United States
Products
BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 25 x 26 mL applicators/case, NDC 54365-400-39, catalog number 930825NS, b) 50 x 26 mL applicators/case, NDC 54365-400-39, bulk catalog number 930825NSB; STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0650-2026More CareFusion recalls
- FDA-Drug2026-07-22BD ChloraPrep Clear skin antiseptic recalled for potential sterility packaging defect
- FDA-Drug2026-07-08BD ChloraPrep Clear skin antiseptic recalled for lack of sterility assurance
- FDA-Drug2026-07-08BD ChloraPrep Hi-Lite Orange recalled for lack of sterility assurance
- FDA-Drug2026-07-08BD ChloraPrep Scrub Teal recalled for lack of sterility assurance
- FDA-Drug2026-07-08BD ChloraPrep Hi-Lite Orange skin antiseptic recalled for lack of sterility assurance
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