Drug recall
NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually…
FDA recall event 74834 · Class II · Medtronic Xomed, Inc.
Key facts
| Event ID | 74834 |
|---|---|
| Recall numbers | Z-0901-2017 |
| Recalling firm | Medtronic Xomed, Inc. |
| Product type | Devices |
| Products | NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Wire in tubing can become exposed, posing potential harm to the intubated patient. |
| Initiation date | Jun 28, 2016 |
| Report date | Jan 4, 2017 |
| Termination date | Aug 7, 2019 |
| City | Jacksonville |
| State | FL |
| Country | United States |
| FEI number | 1045254 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: