Neurovision Medical Products Inc 2024-09-04 Health serious FDA
Health · FDA · Recall #FDA-Z-2719-2024
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx… Recall
Issued September 4, 2024 · Neurovision Medical Products Inc
In September 2024, Neurovision Medical Products Inc recalled the Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
What you should do
- 1 Stop using Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Neurovision Medical Products Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Neurovision Medical Products Inc
- Category
- Health
- Recall date
- September 4, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-2719-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Neurovision Medical Products Inc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.