Home/Recalls/FDA-D-0518-2026
FDA DrugsClass II

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alc...

Published: May 13, 2026Recall ID: D-0518-2026Category: drugsCountry: US

Reason for Recall / Hazard

Lack of assurance of Sterility: potential product contamination

Product Description & Identification

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 fl. oz. (10.5 mL) x 25 applicators per box. Carefusion 213, LLC, El Paso, TX 79912, subsidary of Becton Dickinson and Co. NDC 54365-014-41

Additional Source Details

FieldValue
CityEl Paso
StateTX
Openfda › Nui › 1N0000175486
Openfda › Nui › 2M0011640
Openfda › Unii › 1ND2M416302
Openfda › Unii › 285H0HZU99M
Openfda › RouteTOPICAL
Openfda › Rxcui1052725
Openfda › Spl id40add5c5-68aa-96f9-e063-6294a90a7282
Openfda › Brand namePURPREP
Openfda › Spl set ida1c6e118-7861-c8d0-e053-2995a90aeaaa
Openfda › Package ndc › 154365-014-42
Openfda › Package ndc › 254365-014-41
Openfda › Product ndc54365-014
Openfda › Generic namePOVIDONE IODINE AND ISOPROPYL ALCOHOL
Openfda › Product typeHUMAN OTC DRUG
Openfda › Pharm class csIodine [CS]
Openfda › Substance name › 1ISOPROPYL ALCOHOL
Openfda › Substance name › 2POVIDONE-IODINE
Openfda › Pharm class epcAntiseptic [EPC]
Openfda › Manufacturer nameCareFusion 213 LLC
Openfda › Application number505G(a)(3)
Openfda › Is original packagertrue
Event id98790
Address 11550 Northwestern Dr
Code infoLots# 4263873, Exp. Date 08-31-2026, 4320590, Exp. Date 09-30-2026, 4320591, Exp. Date 10-31-2026.
Postal code79912-8000
Report date20260513
Product typeDrugs
Reason for recallLack of assurance of Sterility: potential product contamination
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260422
Initial firm notificationLetter
Center classification date20260505

Overview

  • Recalling FirmCareFusion 213, LLC
  • StatusOngoing
  • Risk LevelClass II
  • DistributionNationwide in the USA
Official Agency Alert