Neurovision Medical Products Inc: Medical Device Recall in 2024 - (Recall #: Z-2719-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 1, 2024

Date Posted: September 4, 2024

Recall Number: Z-2719-2024

Event ID: 94931

Reason for Recall:

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

Status: Ongoing

Product Quantity: 5 BOXES (25 single kits)

Code Information:

LOT: 051724B/ UDI: B006LTE7003PS52

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated