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Class 2 Device Recall lnvatec SpA brand Diver C.E |
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Date Initiated by Firm |
March 04, 2009 |
Date Posted |
June 07, 2013 |
Recall Status1 |
Terminated 3 on June 10, 2013 |
Recall Number |
Z-1517-2013 |
Recall Event ID |
65289 |
510(K)Number |
K051917 K050276
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Product Classification |
Catheter, embolectomy - Product Code DXE
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Product |
lnvatec SpA brand Diver C.E., Model/Catalog Numbers: DVR010014145, DVR011014145,
Product is manufactured by lnvatec SpA, Roncadelle, Italy, and distributed by Invatec, Inc., Bethlehem, PA and by Medtronic Endovascular Therapies, Santa Rosa, CA The Diver C.E. product is an aspiration catheter indicated for the removal of fresh, soft emboli and thrombi from vessels in the arterial system. |
Code Information |
Serial Numbers/Batches: OPI05931901, OPI05684401, OPI05684501, OPI05684601, OPI05684701, OPI05684801 |
Recalling Firm/ Manufacturer |
Invatec Llc 3101 Emrick Blvd Bethlehem PA 18020-8037
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For Additional Information Contact |
Jonathan Morris 707-566-1143
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Manufacturer Reason for Recall |
Devices labeled for an intended use was not included in the existing 510(k) or PMA, in that, the Indications for use was modified.
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FDA Determined Cause 2 |
Labeling False and Misleading |
Action |
Invatec sent an Urgent - Device Field Action letter dated March 4, 2009, to all affected customer. The letter identified the product, the problem, and the action to be taken by the customer. Customers were required to return a confirmation form, acknowledging the action taken, and identifying affected units in their inventory for return of the product for replacement. The firm indicated that this recall was fully executed in 2009, and this 806 captures the events that took place at that time.
For questions regarding this recall call 707-566-1143. |
Quantity in Commerce |
177 units |
Distribution |
Nationwide 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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510(K) Database |
510(K)s with Product Code = DXE and Original Applicant = INVATEC INNOVATIVE TECHNOLOGIES, S.R.L.
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