CareFusion 213, LLC 2026-05-13 Health serious FDA
Health · FDA · Recall #FDA-D-0517-2026
BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol… Recall
Issued May 13, 2026 · CareFusion 213, LLC
In May 2026, CareFusion 213, LLC recalled the BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Lack of assurance of Sterility: potential product contamination
What you should do
- 1 Stop using BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact CareFusion 213, LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- CareFusion 213, LLC
- Category
- Health
- Recall date
- May 13, 2026
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0517-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- CareFusion 213, LLC has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.