FDAFDA · Food and drugs·Recall number Z-2719-2024
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Published September 4, 2024 · Recall initiated: July 1, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Neurovision Medical Products Inc
- Distributor
- US Nationwide distribution.
- Lot
- LOT: 051724B/ UDI: B006LTE7003PS52
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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