Cobra — Class II medical device recall Z-2719-2024
Ongoing recall by Neurovision Medical Products Inc, reported 2024-09-04, distributed nationwide. mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
| Recall number | Z-2719-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Neurovision Medical Products Inc, Ventura, CA, United States |
| Recall initiated | 2024-07-01 |
| Classified | 2024-08-23 |
| Reported by FDA | 2024-09-04 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| Lot numbers | 051724B |
| Model numbers | LTE7003PM |
Product
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Reason for recall
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
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-2719-2024. 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.