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U.S. Department of Health and Human Services

Class 2 Device Recall Neurovision Ink Printed Endotracheal Tube Electrode. LETEIP1, LETEIP2

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  Class 2 Device Recall Neurovision Ink Printed Endotracheal Tube Electrode. LETEIP1, LETEIP2 see related information
Date Initiated by Firm July 21, 2020
Create Date August 27, 2020
Recall Status1 Terminated 3 on April 30, 2021
Recall Number Z-2902-2020
Recall Event ID 86102
510(K)Number K110989  
Product Classification Stimulator, nerve - Product Code ETN
Product Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 8.0 mm, REF NVTKIT-C8-5, Rx Only, Sterile
UDIB006NVTKITC852/$$7062118C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient ventilation during surgical or parasurgical care using any compatible nerve monitoring system.
Code Information Kit Lots: 012320C 012720C 012820B 012920C 013020C 020720D 021020D 021320E 021420B 021420D 021820B 031220A 031620C 041620A 052120C 060820F 061120B 111319C 120219G 120619A 121819B 121919F 122319B 122719A 123019A 072919B 073019A 073119B 010820E 090419A 112619A 101019B 102319B 102819A 102919A 103019A 103119A 111219F 112619G 112719C 120219F 060420A 062920A
Recalling Firm/
Manufacturer		 Neurovision Medical Products Inc
2443 Portola Rd
Ventura CA 93003-7726
For Additional Information Contact Kevin Rea
866-815-6999
Manufacturer Reason
for Recall		 The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable.
FDA Determined
Cause 2		 Under Investigation by firm
Action Urgent Medical Device Recall Notice, dated July 17, 2020 was sent via email on 7/21/20 and a hard copy via USPS first class mail on 7/28/20-7/29/20 to consignees advising them that Neurovision Medical Products (hereafter NMP) is voluntarily recalling Cobra 1 & 2-Channel EMG Endotracheal Tube, 6 mm, 7 mm, and 8 mm which is used for continuous EMG monitoring and status assessment of the nerves. NMP has initiated this removal due to the potential degradation of the electrode insulation material sooner than the established shelf life. This could make the electrode more susceptible to damage by dental scratching or acute bending. This may interfere with the EMG performance of the device. Failure of the device could result in a delay in the surgical procedure. Malfunction during clinical use should be evident to the clinical user by intermittent or loss of EMG signal and high electrode impedance values. We are aware of one product failure and one complaint associated with the problem. It advises customers to immediately take the following actions: Review the enclosed list of affected lots and product codes. 2. Quarantine product subject to this notice. 3. Cease distribution and use of any product from the affected lots. 4. Advise all applicable departments (including Anesthesia, OR Leadership and Materials Management). 5. Complete and return the enclosed response form as soon as possible: a. Email: customer_service@neurovisionmedical.com b. Fax: (877) 330-1727 6. NMP Customer Service will respond with a return authorization (RMA) number and return shipping label for any stock of affected lots that you may have. 7. If you have distributed this product to another location or entity, notify them of this product recall (include a copy of this notice), and contact NMP Customer Service for a return authorization (RMA). The letter stated the firm is working quickly and closely with their manufacturing team to address the issue. In the meantime, they do have an alt
Quantity in Commerce 1,239
Distribution Worldwide distribution - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, MA, MD, MI, MN, MO, MS, NE, NY, OH, OR, PA, SC, SD, TN, TX, WA, WI and the countries of Canada, Dominican Republic, Hong Kong.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = ETN and Original Applicant = NEUROVISION MEDICAL PRODUCTS, INC.
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