# FDA recall Z-2719-2024

> **Neurovision Medical Products Inc** · Class II · device recall initiated 2024-07-01.

## Product

Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO

## Reason for recall

mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2719-2024
- **Recalling firm:** Neurovision Medical Products Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-01
- **Report date:** 2024-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ventura, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2719-2024

## Citation

> AI Analytics. FDA recall Z-2719-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2719-2024. Source: US FDA. Licensed CC0.

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