Drug recall
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
FDA recall event 94931 · Class II · Neurovision Medical Products Inc
Key facts
| Event ID | 94931 |
|---|---|
| Recall numbers | Z-2719-2024 |
| Recalling firm | Neurovision Medical Products Inc |
| Product type | Devices |
| Products | Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size. |
| Initiation date | Jul 1, 2024 |
| Report date | Sep 4, 2024 |
| City | Ventura |
| State | CA |
| Country | United States |
| FEI number | 1930870 |
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: