FDA Device recall Z-2719-2024
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
- FDA Device
- Class II
- ongoing
- Published 2024-09-04
On 2024-09-04 the FDA classified a Class II recall of Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO by Neurovision Medical Products, citing mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2719-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-07-01 |
| Published | 2024-09-04 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Neurovision Medical Products |
| Distribution | US |
Product
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Reason
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Identifiers
| code_info | LOT: 051724B/ UDI: B006LTE7003PS52 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2719-2024%22
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