# FDA recall Z-2249-2025

> **AVID Medical, Inc.** · Class II · device recall initiated 2025-06-11.

## Product

GS ENDOSCOPY PACK. Medical convenience kit.

## Reason for recall

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

## Distribution

Domestic: CA, IL, MD, OH, PA, TX, WA.

## Key facts

- **Recall number:** Z-2249-2025
- **Recalling firm:** AVID Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-11
- **Report date:** 2025-08-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Toano, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2249-2025

## Citation

> AI Analytics. FDA recall Z-2249-2025. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2249-2025. Source: US FDA. Licensed CC0.

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