# FDA recall Z-0051-2021

> **Ansell Healthcare Products LLC** · Class II · device recall initiated 2020-08-19.

## Product

MICROFLEX Diamond Grip Examination Gloves, MF-300 - Product Usage: A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner s hand or finger to prevent contamination between patient and examiner.

## Reason for recall

Examination gloves were shipped inadvertently, without to verify barrier integrity.

## Distribution

U.S. Nationwide distribution including in the states of IL, OK, WI, PA, TX, OH, MI, IN, VA, AR, KS, MO, NV, OR, FL, QC, NJ, NE, KY, AL, TN, LA, NY, SC, MS, MD, CA, GA, SD.

## Key facts

- **Recall number:** Z-0051-2021
- **Recalling firm:** Ansell Healthcare Products LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-08-19
- **Report date:** 2020-10-14
- **Termination date:** 2021-11-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Reno, NV, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0051-2021

## Citation

> AI Analytics. FDA recall Z-0051-2021. Retrieved 2026-09-08 from https://api.ai-analytics.org/recall/Z-0051-2021. Source: US FDA. Licensed CC0.

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