# FDA recall Z-2520-2025

> **O&M HALYARD INC** · Class II · device recall initiated 2025-07-17.

## Product

Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029   Universal Pack, Model: 77165-06  AC2424902B 09/05/2029

## Reason for recall

Surgical drape packs may have open seals, which may compromise the sterility of the product.

## Distribution

Worldwide - US Nationwide distribution in the states of GA, AL, PA and the countries of MX.

## Key facts

- **Recall number:** Z-2520-2025
- **Recalling firm:** O&M HALYARD INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-17
- **Report date:** 2025-09-10

- **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-2520-2025

## Citation

> AI Analytics. FDA recall Z-2520-2025. Retrieved 2026-08-19 from https://api.ai-analytics.org/recall/Z-2520-2025. Source: US FDA. Licensed CC0.

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