DuraPrep Surgical Solution Iodine Povacrylex — Class II drug recall D-1417-2015
Terminated recall by 3M Company - Health Care Business, reported 2015-09-16, distributed nationwide. Chemical contamination: Product may be contaminated with a toxic compound.
| Recall number | D-1417-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | 3M Company - Health Care Business, Saint Paul, MN, United States |
| Recall initiated | 2015-08-06 |
| Classified | 2015-09-08 |
| Reported by FDA | 2015-09-16 |
| Terminated | 2017-03-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, MX, MY, PA, PE |
| Reason classes | chemical contamination |
| NDC | 17518-0011-07, 17518-0011-08 |
| Expiration dates | 2016-08-31, 2016-09-30 |
Product
DuraPrep Surgical Solution Iodine Povacrylex (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) Patient Preoperative Skin Preparation, supplied in a) 0.9 fl oz, 26 mL Single Use Applicator w/urethane sponge and 2-count Cotton-tipped swabs per pouch, packaged in 20 pouches per case (NDC 17518-0011-08, UPC (01) 0 03 17518 01108 5) and b) 0.2 fl oz, 6 mL Single Use Applicator w/urethane sponge per pouch, packaged in 50 pouches per case (NDC 17518-0011-07, UPC (01) 0 03 17518 01107 8), OTC, Made in U.S.A. by 3M Health Care, 2510 Conway Ave., St. Paul, MN 55144.
Reason for recall
Chemical contamination: Product may be contaminated with a toxic compound.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1417-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.