Class II — Neurovision Medical Products Inc
| Recalling firm | NEUROVISION MEDICAL PRODUCTS, INC. |
|---|---|
| Registered facility | NEUROVISION MEDICAL PRODUCTS, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size. |
| Product | Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO |
| Quantity | 5 BOXES (25 single kits) |
| Distribution | US Nationwide distribution. |
| Initiated | 2024-07-01 |
| Classified | 2024-08-23 |
| Recall number | Z-2719-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Neurovision Medical Products Inc (Z-2719-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94931/
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