# FDA recall Z-0609-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2017-09-11.

## Product

BlockAid Cut Resistant Surgical Glove Liners, combine stainless steel and synthetic fibers woven together to form a cut resistant glove material. Blockaid Cut Resistant Surgical Glove Liners are to be worn between two layers of surgical gloves. Item Number: 650126, 650127, 650128, 650129, 650130, 650131

## Reason for recall

Cut resistant surgical glove liners lack sterility assurance.

## Distribution

Distributed in 29 states: AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, MI, MO, MT, NC, NE, NJ, NY, OH, OR, PA, SC, TN, TX, VA, WV and Washington, DC. Distributed to 1 Veteran's Administration hospital in MO. Distributed in Netherland, Peru, and Switzerland.

## Key facts

- **Recall number:** Z-0609-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-11
- **Report date:** 2018-02-21
- **Termination date:** 2018-08-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0609-2018

## Citation

> AI Analytics. FDA recall Z-0609-2018. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0609-2018. Source: US FDA. Licensed CC0.

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