# FDA recall Z-0929-2026

> **AVID Medical, Inc.** · Class II · device recall initiated 2025-11-14.

## Product

Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.

## Reason for recall

Potential for incomplete seal on header bag.

## Distribution

US distribution to GA, IL, NE, MD.

## Key facts

- **Recall number:** Z-0929-2026
- **Recalling firm:** AVID Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-14
- **Report date:** 2025-12-24

- **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-0929-2026

## Citation

> AI Analytics. FDA recall Z-0929-2026. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0929-2026. Source: US FDA. Licensed CC0.

---

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