# FDA recall D-0261-2018

> **Medline Industries Inc** · Class II · drug recall initiated 2017-09-21.

## Product

Medline CNTRL Line Removal Kit Scripps. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093

## Reason for recall

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads  is below label claim of 0.85%.

## Distribution

Nationwide USA, Puerto Rico, China, Chile, Guam, Honduras, India, Israel, Malaysia, Mexico, Turkey

## Key facts

- **Recall number:** D-0261-2018
- **Recalling firm:** Medline Industries Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-09-21
- **Report date:** 2018-02-07
- **Termination date:** 2023-08-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0261-2018

## Citation

> AI Analytics. FDA recall D-0261-2018. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0261-2018. Source: US FDA. Licensed CC0.

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