# FDA recall Z-0295-2018

> **Medline Industries Inc** · Class II · device recall initiated 2017-07-18.

## Product

Sterile Elastic Esmark Bandage, 3" x 9", individually packaged in a Tyvek plastic form fill seal pouch and placed into a corrugate case, 20 individually packed bandages per case.

## Reason for recall

Product did not undergo correct sterilization procedures and may potentially be non-sterile.

## Distribution

Worldwide Distribution - US Nationwide in the states of AK, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, NC, NH, NJ, NY, OH, OK, OR, PA, TN, TX, WA and the countries of Canada, Saudi Arabia, and Netherlands.

## Key facts

- **Recall number:** Z-0295-2018
- **Recalling firm:** Medline Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-18
- **Report date:** 2018-01-03
- **Termination date:** 2020-04-24

- **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=Z-0295-2018

## Citation

> AI Analytics. FDA recall Z-0295-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0295-2018. Source: US FDA. Licensed CC0.

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