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Neurovision Medical Products Inc Recall 94931

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

Neurovision Medical Products Inc Recall 94931 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-2719-2024
Event ID94931
Event DescriptionCobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Product TypeDevices
DistributionUS Nationwide distribution.
Quantity5 BOXES (25 single kits)
Recall Reasonmislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Device Classification20240904
Device Code InfoLOT: 051724B/ UDI: B006LTE7003PS52
Center Classification Date20240823
Recall Initiation Date20240701
Recalling FirmNeurovision Medical Products Inc
Initial Notification Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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