Date Initiated by Firm |
February 21, 2020 |
Date Posted |
April 16, 2020 |
Recall Status1 |
Terminated 3 on January 28, 2021 |
Recall Number |
Z-1849-2020 |
Recall Event ID |
85339 |
510(K)Number |
K041021
|
Product Classification |
Probe, radiofrequency lesion - Product Code GXI
|
Product |
R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 - Product Usage: The Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain. |
Code Information |
Catalog #257-1810 Sterile Lot #/Expiration Date/ 1. 14108679/exp. 3-29-23/ 2. 14109199/exp. 1-21-24/ 3. 14108568/exp. 2-4-23/ Catalog #257-1810D Sterile Lot #/Expiration Date/ 1. 14109199/ exp. 1-21-24/ 2. 14109690/exp. 9-26-24/ |
Recalling Firm/ Manufacturer |
Epimed International 13958 Diplomat Dr Farmers Branch TX 75234-8805
|
For Additional Information Contact |
Bobbi Harrington 518-848-3901 Ext. 1200
|
Manufacturer Reason for Recall |
Incorrect expiration date on introduction cannula packaging.
|
FDA Determined Cause 2 |
Labeling design |
Action |
On 02/21/2020, URGENT: MEDICAL DEVICE RECALL letters were sent to customers by way of Standard U.S. Mail services. |
Quantity in Commerce |
1374 |
Distribution |
Worldwide distribution - US Nationwide distribution including the states of AL, CA, FL, GA, IL, MD,MI, MS, NJ, NY, OK, TN, TX, WA and WY and the countries of Australia, Chile, United Kingdom. |
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 = GXI and Original Applicant = EPIMED INTERNATIONAL, INC.
|