# FDA recall Z-2230-2026

> **O&M HALYARD INC** · Class II · device recall initiated 2026-04-13.

## Product

Halyard Purezero Ultraviolet Nitrile Exam Gloves  Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)

## Reason for recall

Nitrile Exam Glove failed to meet specifications  chemical permeation performance.

## Distribution

US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC.

## Key facts

- **Recall number:** Z-2230-2026
- **Recalling firm:** O&M HALYARD INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-13
- **Report date:** 2026-06-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Alpharetta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2230-2026

## Citation

> MORVS. FDA recall Z-2230-2026. Retrieved 2026-10-16 from https://api.morvs.ai/recall/Z-2230-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*