# FDA recall Z-3151-2026

> **AVID Medical, Inc.** · Class I · device recall initiated 2026-08-10.

## Product

Haylard 18G SINGLE SHOT EPI TRAY;   Model/Item Number (Kit): DPGE002-02;

## Reason for recall

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

## Distribution

Domestic: IL, NC, VA, WY;

## Key facts

- **Recall number:** Z-3151-2026
- **Recalling firm:** AVID Medical, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-08-10
- **Report date:** 2026-09-23

- **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-3151-2026

## Citation

> MORVS. FDA recall Z-3151-2026. Retrieved 2026-10-17 from https://api.morvs.ai/recall/Z-3151-2026. Source: US FDA. Licensed CC0.

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