NIM TriVantage EMG Endotracheal Tubes — Class II medical device recall Z-0696-2024
Ongoing recall by Medtronic Xomed, Inc., reported 2024-01-17. Firm received reports of customers experiencing noise from the NIM System, lead-off or high impedance issues,
| Recall number | Z-0696-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Xomed, Inc., Jacksonville, FL, United States |
| Recall initiated | 2023-11-07 |
| Classified | 2024-01-10 |
| Reported by FDA | 2024-01-17 |
| Quantity | 80,569 units |
| UPC / GTIN / UDI-DI | 00643169373099, 00643169373105, 00643169782587, 00643169782594, 00763000033941, 00763000033958, 00763000033965, 00763000041526, 20763000041513, 20763000041520, 20763000041537 |
| Serial numbers | 0225750658, 0225784378, 0225784379, 0225784380, 0225784381, 0225784382, 0225784383, 0225784384, 0225784385, 0225785080, 0225785081, 0225785083, 0225785085, 0225785406, 0225785407, 0225785408, 0225785410, 0225785421, 0225785422, 0225785423, 0225785424, 0225785425, 0225785466, 0225785467, 0225785468 and 207 more |
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,
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0696-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.