|
Class 1 Device Recall Catheter introducer |
|
Date Initiated by Firm |
December 17, 2010 |
Date Posted |
January 28, 2011 |
Recall Status1 |
Terminated 3 on July 11, 2011 |
Recall Number |
Z-0941-2011 |
Recall Event ID |
57540 |
510(K)Number |
K082063
|
Product Classification |
Introducer, catheter - Product Code DYB
|
Product |
Prelude Short Sheath Introducer, 7F-SMT, 4 cm, REF No: PSS-7F-4-038MT, Sterile EO, Merit Medical, South Jordan, Utah. Intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries while maintaining hemostasis for a variety of diagnostic and therapeutic procedures. Can also provide access to a native or synthetic graft used for hemodialysis. |
Code Information |
Lot Number: H179575 |
Recalling Firm/ Manufacturer |
Merit Medical Systems, Inc. 1600 West Merit Parkway South Jordan UT 84095
|
For Additional Information Contact |
801-316-4932
|
Manufacturer Reason for Recall |
Introducer tips may detach and embolize during use, or the tip material may elicit a thrombogenic response.
|
FDA Determined Cause 2 |
Component change control |
Action |
Merit Medical Systems, Inc., issued an "Urgent Product Recall Notice" dated December 17, 2010, and contacted all customers (sales reps and authorized distributors) via email, phone and/or fax. The notice described the product, problem and action to be taken by the customers (Sales reps/Distributors). The customers were instructed to contact all their customers to identify, quarantine and return all unused inventory and extend the recall to any of their customers who may have received the affected products. The customers were instructed to complete and return the Manufacturer RECALL NOTIFICATION and Product Retrieval Form via fax to 1-801-208-3378 and send original to: the Manager, Customer Service, Merit Medical Systems, Inc., 1600 West Merit Parkway, South Jordan, UT 84095-2416.
Questions should be directed to the Senior Product Manager at 801-208-4344 or the Manager, Customer Service at 801-208-4365. |
Quantity in Commerce |
378 units |
Distribution |
Nationwide Distribution |
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 = DYB and Original Applicant = MERIT MEDICAL SYSTEMS, INC.
|
|
|
|