NIM TRIVANTAGE EMG Endotracheal Tube — Class II medical device recall Z-0743-2022
Ongoing recall by Medtronic Xomed, Inc., reported 2022-03-16, distributed nationwide. There is potential for multiple issues due to a manufacturing nonconformity.
| Recall number | Z-0743-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Xomed, Inc., Jacksonville, FL, United States |
| Recall initiated | 2021-12-22 |
| Classified | 2022-03-10 |
| Reported by FDA | 2022-03-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BD, BE, BH, BR, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DK, DO, DZ, ES, FI, FR, GB, GR, GT, HK, HR, HU, IE, IL, IN, IS, IT, JP, KR, KW, LB, LU, MA, MX, MY, NL, NO, NZ, PA, PH, PL, PT, QA, RO, RS, RU, SA, SE, SG, SK, TH, TW, VN, ZA |
| Quantity | 301,926 devices |
| UPC / GTIN / UDI-DI | 00763000033934, 00763000033941, 00763000033958, 00763000033965, 00763000033972, 20763000041506, 20763000041513, 20763000041520, 20763000041537, 20763000041544 |
| Lot numbers | 0010791039, 0218275302, 0218275305, 0218275886, 0218452814, 0218452815, 0218496850, 0218515807, 0218540733, 0218540734, 0218540735, 0218663943, 0218663944, 0218664146, 0218664148, 0218664149, 0218664150, 0218664151, 0218664152, 0218664153, 0218664154, 0218664155, 0218664156, 0218664157, 0218664158, 0218664159, 0218664160, 0218664161, 0218664162, 0218664163, 0218762694, 0218762695, 0218762697, 0218762698, 0218762699, 0218762700, 0218762701, 0218762702, 0218762703, 0218762704 and 460 more |
Product
NIM TRIVANTAGE EMG Endotracheal Tube
Reason for recall
There is potential for multiple issues due to a manufacturing nonconformity.
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-0743-2022. 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.