Class II

Medical Device Recall: Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO

Neurovision Medical Products Inc · July 1, 2024

Reason for Recall

mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

5 BOXES (25 single kits)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2719-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Neurovision Medical Products Inc Medical Device Recall: Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO | SafeCheck