# FDA recall Z-0696-2024

> **Medtronic Xomed, Inc.** · Class II · device recall initiated 2023-11-07.

## Product

NIM TriVantage EMG Endotracheal Tubes, Model (REF) Numbers and sizes:  a) 8229706, 6.0MM ID;   b) 8229707, 7.0MM ID;   c) 8229708, 8.0MM ID;   d) 8229736, 6MM ID 3PK;   e) 8229737, 7MM ID 3 PK;   f) 8229738, 8MM ID 3 PK

## Reason for recall

Firm received reports of customers experiencing noise from the NIM System, lead-off or high impedance issues, or loss of/intermittent nerve monitoring,

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-0696-2024
- **Recalling firm:** Medtronic Xomed, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-07
- **Report date:** 2024-01-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Jacksonville, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0696-2024

## Citation

> AI Analytics. FDA recall Z-0696-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0696-2024. Source: US FDA. Licensed CC0.

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