# FDA recall Z-3194-2026

> **AVID Medical, Inc.** · Class I · device recall initiated 2026-07-22.

## Product

Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator.  Kit Model Number: KRIV26-02.

## Reason for recall

Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-3194-2026
- **Recalling firm:** AVID Medical, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-22
- **Report date:** 2026-09-30

- **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-3194-2026

## Citation

> MORVS. FDA recall Z-3194-2026. Retrieved 2026-10-23 from https://api.morvs.ai/recall/Z-3194-2026. Source: US FDA. Licensed CC0.

---

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