FDAJuly 1, 2024device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

neurovision medical productsneurovisionneurovision medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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