Recall StatusTerminated
Date Initiated2019-05-30
Date Terminated2021-04-28
Product Quantity118 units
Reason for Recall
The firm initiated a voluntary correction of certain Cosman TCN Electrodes due to an incorrect revision of the Instructions for Use (IFU) being packaged with these products.
Firm Action
The firm reported that they have included replacement IFUs with the notification package and these were sent Fedex 2 Day mail. The following was included in the firm's notification letter: "Your local Sales Representative can answer any questions that you may have regarding this correction. Please pass this notice to any healthcare professional from your organization who needs to be aware and to any organization where the potentially affected devices have been transferred (if appropriate). Please provide details of any affected devices that have been transferred to other organizations (if appropriate).
The Reply Verification Tracking Form enclosed with the Notice must be completed and returned even if you do not have any affected units in your inventory.
1.Complete and return the Reply Verification Tracking Form (RVTF).
Complete the enclosed Reply Verification Tracking Form even if you do not have any affected product to be corrected. Follow the directions on this page and on the Reply Verification Tracking Form.
Verify if the product within your inventory is affected. If so, indicate on your Verification Form the part and lot number(s) in your possession.
Email or fax the Reply Verification Tracking Form to the Field Action Center as described below:
Email:
[email protected]
or Fax to: Field Action Center 1-866-213-1806
Please email or fax your Reply Verification Tracking Form(s) immediately.
2. Place the included replacement IFUs with any affected product you have identified in your inventory.
IFUs originally included with affected products must be discarded."
Root Cause
Error in labeling
Distribution Pattern
US Nationwide distribution in the states of AZ, CA,CO, FL,GA, ID,IL, IN, KY, MA, MD, MI, MO, NV, NY, OH, OK, OR, SC, TX, UT, VA, WA, and WI.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.