Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Reported: September 4, 2024 Initiated: July 1, 2024 #Z-2719-2024
Product Description
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Reason for Recall
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Details
- Recalling Firm
- Neurovision Medical Products Inc
- Units Affected
- 5 BOXES (25 single kits)
- Distribution
- US Nationwide distribution.
- Location
- Ventura, CA
Frequently Asked Questions
What product was recalled? ▼
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO. Recalled by Neurovision Medical Products Inc. Units affected: 5 BOXES (25 single kits).
Why was this product recalled? ▼
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 4, 2024. Severity: Moderate. Recall number: Z-2719-2024.
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