ANGIODYNAMICS PROFILER BALLOON DILATATION CATHETER, Catalog No./REF 16801101, BALLOON DIAMETER 4MM, BALLOON LENGTH 2 CM, CATHETER LENGTH 40 CM, STERILE, MANUFACTURED IN USA AngioDynamics 603 Queensbury Avenue, Queensbury, NY 12804 Cardiovascular catheterization
FDA Recall Z-3261-2011 · Posted 2011-09-19
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Recalling FirmAngiodynamics Worldwide Headquarters
Recall StatusTerminated
Product CodeDQY
Date Initiated2011-02-25
Date Terminated2012-10-18
Product Quantity15 units
Reason for Recall
The particular lots of Profiler PTA Balloon Catheters were labeled incorrectly. Lot 532109 contains product that is actually 5 mm x 4 cm x 40 cm and Lot 532794 contains product that is actually 4 mm x 2 cm x 40 cm.
Firm Action
Angiodynamics, Inc sent a "Urgent Medical Device Recall letter" dated February 25, 2011 to all affected customers via Certified Mail Return Receipt Requested. The letter identified the product the problem and the action
needed to be taken by the customer.
The customer was instructed the following steps
1. Identify and segregate the recalled lot that is in your possession.
2. Complete the enclosed Profiler PTA Balloon Catheter Recall Reply Form and fax it to the attention of the Profiler PTA Balloon Catheter Recall Coordinator at 518-798-1360.
The form lists the catalog numbers, lot numbers, and quantity our records indicate your facility has received.
For further questions please call 1-800-772-6446.
Root Cause
Employee error
Distribution Pattern
Nationwide Distribution including the states of CA, GA, ID, MI, OH and PA.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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