Medtronic Vascular Pioneer Catheter (Crosspoint TransAccess Catheter); Model TA-XP-001; Product is manufactured and distributed by Medtronic Vascular, Santa Rosa, CA 95403 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pioneer Catheter (Crosspoint TransAccess Catheter); Model TA-XP-001; Product is manufactured and distributed by Medtronic Vascular, Santa Rosa, CA 95403
Brand
Medtronic Vascular
Lot Codes / Batch Numbers
All Codes.
Products Sold
All Codes.
Medtronic Vascular is recalling Pioneer Catheter (Crosspoint TransAccess Catheter); Model TA-XP-001; Product is manufactured and dis due to Sterility may be compromised as evidenced by a loss of package integrity.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterility may be compromised as evidenced by a loss of package integrity.
Recommended Action
Per FDA guidance
On 11/1/06, the firm issued letters via Federal Express to all its direct consignees, informing them of the affected product and providing instructions on the recall.
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