Date Initiated by Firm |
July 18, 2014 |
Date Posted |
August 13, 2014 |
Recall Status1 |
Terminated 3 on February 05, 2015 |
Recall Number |
Z-2206-2014 |
Recall Event ID |
68788 |
Product Classification |
Apparatus, hemoperfusion, sorbent - Product Code FLD
|
Product |
PrisMARS Kit (component of MARS Treatment Kit Type 1115/1 PrisMARS US), 1 MARS Treatment Kit per carton box, Product Number 800480, Batch |
Code Information |
Model Number MARS Treatment Kit Type 1115/1 PrisMARS US, Batch 0000017412 - 0000019827, Expiry Date 06/2014 to 05/2016 |
Recalling Firm/ Manufacturer |
Gambro Renal Products, Incorporated 14143 Denver West Pkwy Lakewood CO 80401-3266
|
For Additional Information Contact |
Thomas W. Dielmann 303-232-6800
|
Manufacturer Reason for Recall |
Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.
|
FDA Determined Cause 2 |
Device Design |
Action |
Gambro sent an Urgent Field Safety Notice dated July 18, 2014 to all end-users. A Customer Reply Form was attached to the notice for customers to complete and return. |
Quantity in Commerce |
401,451 |
Distribution |
Worldwide Distribution. |
Total Product Life Cycle |
TPLC Device Report
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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.
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