Purprep recalls

Purprep products have been recalled 3 times, most recently on 8 Jul 2026. The recalling company is usually CareFusion 213. The most common reason is sterility.

Total recalls3since 2026

Last 12 months3reported

Class I00% of total

Ongoing3latest 8 Jul 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 2May 0 1 0Aug 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why purprep is recalled

Sterility3100%

Companies

CareFusion 2133100%

By year

20263100%

Ongoing purprep recalls

3 active

Reported	Class	Recall	Company	Reason	Where
8 Jul 2026Drug	CLASS II	BD PurPrep, (Povidone-iodine 8.3% w/w recalled by CareFusion 213Purprep	CareFusion 213	Sterility	Nationwide
13 May 2026Drug	CLASS II	BD PurPrep, Povidone-iodine 8.3% w/w recalled by CareFusion 213Purprep	CareFusion 213	Sterility	Nationwide
13 May 2026Drug	CLASS II	BD PurPrep, Povidone-iodine 8.3% w/w recalled by CareFusion 213Purprep	CareFusion 213	Sterility	Nationwide

All purprep recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
8 Jul 2026Drug	CLASS II	BD PurPrep, (Povidone-iodine 8.3% w/w recalled by CareFusion 213Purprep	CareFusion 213	Sterility	Nationwide
13 May 2026Drug	CLASS II	BD PurPrep, Povidone-iodine 8.3% w/w recalled by CareFusion 213Purprep	CareFusion 213	Sterility	Nationwide
13 May 2026Drug	CLASS II	BD PurPrep, Povidone-iodine 8.3% w/w recalled by CareFusion 213Purprep	CareFusion 213	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.