# FDA recall Z-0162-2018

> **Medline Industries Inc** · Class II · device recall initiated 2017-10-23.

## Product

Sensicare Green Surgical Glove, PI, LF, PF.  Packaged in a poly/poly peel pouch with Sunoco films, sterile.  Surgical glove.

## Reason for recall

Possible open seal on top portion of the package.  Could cause breach of sterility.

## Distribution

Worldwide Distribution - US including AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY.      Internationally to Canada.

## Key facts

- **Recall number:** Z-0162-2018
- **Recalling firm:** Medline Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-10-23
- **Report date:** 2017-11-29
- **Termination date:** 2021-04-06

- **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-0162-2018

## Citation

> AI Analytics. FDA recall Z-0162-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0162-2018. Source: US FDA. Licensed CC0.

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