ev3 The Endovascular Company, IntraCoil Self-Expanding Peripheral Stent, Model REF VT-6-60-135, Lot 4401214, Use Before 2010-07. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ev3 The Endovascular Company, IntraCoil Self-Expanding Peripheral Stent, Model REF VT-6-60-135, Lot 4401214, Use Before 2010-07.
Lot Codes / Batch Numbers
Lot 4401214
Products Sold
Lot 4401214
A medical device manufacturer is recalling ev3 The Endovascular Company, IntraCoil Self-Expanding Peripheral Stent, Model REF VT-6-60-135, Lot due to An IntraCoil 6 mm x 40 mm stent was labeled as a 6 mm x 60 mm stent.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
An IntraCoil 6 mm x 40 mm stent was labeled as a 6 mm x 60 mm stent.
Recommended Action
Per FDA guidance
ev3 representative visited the consignee on 4/15/08 and spoke to the physician at the site that used the device. A Device Recall Field Action Reconcilliation Form was requested.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA
Page updated: Jan 10, 2026