CryoCath Technologies Inc. 16771 Chemin Ste-Marie Kirkland Canada 7F Freezor Cardiac Cryoablation catheter, REF # 207F1. CryoCath Technologies Inc. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
7F Freezor Cardiac Cryoablation catheter, REF # 207F1. CryoCath Technologies Inc.
Brand
CryoCath Technologies Inc. 16771 Chemin Ste-Marie Kirkland Canada
Lot Codes / Batch Numbers
Reference # 207F1, Lot number 00418.
Products Sold
Reference # 207F1, Lot number 00418.
CryoCath Technologies Inc. 16771 Chemin Ste-Marie Kirkland Canada is recalling 7F Freezor Cardiac Cryoablation catheter, REF # 207F1. CryoCath Technologies Inc. due to Outer cartons of catheters were mislabeled with two different reference numbers. The front of the package showed the correct reference number; 207F1,. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Outer cartons of catheters were mislabeled with two different reference numbers. The front of the package showed the correct reference number; 207F1, however the section on the top of the box incorrectly referenced 207F3. All inside labels (inside the box and affixed on device pouches) showed the correct reference number, 207F1.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 08/04/2006.
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