Guidant Corp-Cpi Division Guidant EasyTrak 8 French Guiding Catheter, Inner Diameter .087'', 2.21 mm, Overall Length 54 cm, CS Wide Tip Shape, CS-W, REF 6705 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Guidant EasyTrak 8 French Guiding Catheter, Inner Diameter .087'', 2.21 mm, Overall Length 54 cm, CS Wide Tip Shape, CS-W, REF 6705
Brand
Guidant Corp-Cpi Division
Lot Codes / Batch Numbers
Lots 4012251, 4012451, 4012851, 4012951, 4020451, 4021951, and 4022551
Products Sold
Lots 4012251, 4012451, 4012851, 4012951, 4020451, 4021951, and 4022551
Guidant Corp-Cpi Division is recalling Guidant EasyTrak 8 French Guiding Catheter, Inner Diameter .087'', 2.21 mm, Overall Length 54 cm, CS due to The terminal hub component in a some of the catheters has an unintended abrupt transition between the entry port and the catheter lumen which can re. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The terminal hub component in a some of the catheters has an unintended abrupt transition between the entry port and the catheter lumen which can result in difficulty introducing or removing delivery system components during lead placement.
Recommended Action
Per FDA guidance
Starting on March 11, 2003, the firm''s representatives visited consignees, to whom the recalled catheters had been consigned, and retrieved the catheters.
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 noticePage updated: Jan 10, 2026