# FDA recall D-1417-2015

> **3M Company - Health Care Business** · Class II · drug recall initiated 2015-08-06.

## 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.

## Distribution

Nationwide, Puerto Rico, and to foreign distribution centers in Dominican Repulbic, Malaysia, Mexico, Panama, Peru, and United Arab Emirates.

## Key facts

- **Recall number:** D-1417-2015
- **Recalling firm:** 3M Company - Health Care Business
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-08-06
- **Report date:** 2015-09-16
- **Termination date:** 2017-03-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1417-2015

## Citation

> AI Analytics. FDA recall D-1417-2015. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1417-2015. Source: US FDA. Licensed CC0.

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