---
title: "Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS... — FDA record Z-2230-2026 | Is It on Recall"
description: "Nitrile Exam Glove failed to meet specifications chemical permeation performance."
url: https://isitonrecall.com/recall/fda-device-z-2230-2026-halyard-purezero-ultraviolet-nitrile-exam-gloves-reference-numbers-48771-xs-48772-sm-48773-md-48774/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.)... — FDA record Z-2230-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 13, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)
- **Reason**: Nitrile Exam Glove failed to meet specifications chemical permeation performance.
- **Classification**: Class II
- **Recalling firm**: O&M HALYARD INC
- **Quantity**: 452,500 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2230-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2230-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | REF: 48771/UDI: 30680651487712 (Package)20680651487715 (Primary)90680651487714 (Unit of Use) ; 48772/30680651487729 (Package)20680651487722 (Primary)90680651487721 (Unit of Use);48773/30680651487736 (Package)20680651487739 (Primary)90680651487738 (Unit of Use);48774/UDI: 30680651487743 (Package)20680651487746 (Primary) 90680651487745 (Unit of Use);48775/UDI:30680651487750 (Package)20680651487753 (Primary)90680651487752 (Unit of Use) |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [South Carolina](https://isitonrecall.com/state/south-carolina/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jun 3, 2026
- **Recall initiation date**: Apr 13, 2026
- **Center classification date**: May 22, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2230-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [O&M HALYARD, INC. records](https://isitonrecall.com/brand/o-m-halyard-inc/)
