NIM EMG Endotracheal Tube — Class II medical device recall Z-0901-2017
Terminated recall by Medtronic Xomed, Inc., reported 2017-01-04, distributed nationwide. Wire in tubing can become exposed, posing potential harm to the intubated patient.
| Recall number | Z-0901-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Xomed, Inc., Jacksonville, FL, United States |
| Recall initiated | 2016-06-28 |
| Classified | 2016-12-23 |
| Reported by FDA | 2017-01-04 |
| Terminated | 2019-08-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BE, BR, BS, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DK, DO, DZ, EC, ES, FI, FR, GB, GR, HK, HR, HU, IE, IL, IN, IR, IS, IT, JP, KR, KW, LK, LU, MA, MX, MY, NL, NO, NZ, OM, PA, PE, PL, PT, SA, SE, SG, TR, TT, TW, UA |
| Quantity | 3,752 |
Product
NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
Reason for recall
Wire in tubing can become exposed, posing potential harm to the intubated patient.
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-0901-2017. 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.