Class IIOngoing
BD PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.… recall
FDA recall D-0644-2026 · initiated Jun 11, 2026
By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Jul 8, 2026How we research
CareFusion 213, LLC recalled BD PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl a… in Jun 2026 — an FDA Class II recall (D-0644-2026) 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 PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w), 50 x 26 mL Applicator/case, STERILE SOLUTION, CAREFUSION 213, LLC, EL PASO, TX 79912, subsidiary of Beckton, Dickson and Co, Catalog Number 960120NSB; NDC 54365-014-42.
- 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
Frequently asked
- Was BD PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl a… recalled?
- CareFusion 213, LLC recalled BD PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl a… in Jun 2026 — an FDA Class II recall (D-0644-2026) 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 PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl a… recalled?
- Per the FDA enforcement record, the reason for recall D-0644-2026 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 PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl a… 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 PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl a… 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-0644-2026, initiated Jun 2026.