NIM EMG Endotracheal Tube — Class I medical device recall Z-1521-2022
Ongoing recall by Medtronic Xomed, Inc., reported 2022-09-07, distributed nationwide. The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endo
| Recall number | Z-1521-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Xomed, Inc., Jacksonville, FL, United States |
| Recall initiated | 2022-04-29 |
| Classified | 2022-09-01 |
| Reported by FDA | 2022-09-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BE, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DK, DZ, ES, FI, FR, GB, GR, HK, HR, HU, IE, IL, IN, IR, IS, IT, JP, KR, KW, LK, LT, LU, MX, NL, NO, NZ, OM, PA, PL, PT, QA, RO, SA, SE, SK, TR, TW, VN |
| Quantity | 23,820 units |
| UPC / GTIN / UDI-DI | 00613994415431, 00613994415455, 00613994415462 |
| Model numbers | 8229306J, 8229307J, 8229308J |
Product
NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J
Reason for recall
The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.
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-1521-2022. 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.