FDA Recall Terminated

IntellaTip MiFi XP Temperature Ablation Catheter; 10m x 8F (2.67mm) Asymmetric Curve. The BSC Controller and Accessories are indicated for use in conjunction with standard and high power catheters for cardiac ablation procedures.

Recall: Z-1799-2014 · Initiated May 15, 2014

Recall

Recall Number
Z-1799-2014
Event Number
68373
Firm
Boston Scientific Corporation
FEI Number
2939204
Product Code
OAD
Status
Terminated
Root Cause
Use error
Initiated
May 15, 2014
Posted
June 16, 2014
Terminated
June 25, 2015
Address
47215 Lakeview Blvd, Fremont, CA, 94538-6530

Description

IntellaTip MiFi XP Temperature Ablation Catheter; 10m x 8F (2.67mm) Asymmetric Curve. The BSC Controller and Accessories are indicated for use in conjunction with standard and high power catheters for cardiac ablation procedures.

Reason

Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not manufactured according to specification.

Action

Customers were informed of the recall via overnight letter sent on May 15, 2014.

Distribution

Nationwide Distribution.

Quantity

968 units - all models