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.