ClearanceBrief
Recall Z-1473-2009 ยท DXE Catheter, Embolectomy

Arrow International Inc

Arrow Embolectomy Catheters: 4 French, 2 Lumen x 40cm, Product Number: W01798, Single use, Latex Free, Rx only, Arrow International, 2400 Bernville Road, Reading, PA 19605. The arterial embolectomy catheter is intended for use in removing arterial emboli.

DateJun 25, 2009 (initiated Mar 25, 2009)
StatusTerminated
ReasonThe inflation arm tubing may separate from the stopcock adapter.
Root causeProcess control
ActionArrow International issued an "Urgent Medical Device Recall" letter dated March 25, 2009 describing proper handling of the affected device. Consignees were also instructed to complete a Recall Acknowledgement and Stock Status Form and fax to Arrow International at 1-800-343-2935. Further questions should be directed to Arrow International, Customer Service Department at 1-800-523-8446.
Quantity6910 units (total all three products)
DistributionWorldwide Distribution - USA and Panama.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K902327EMBOLECTOMY CATHETER
Clincal Instruments Corp., Feb 25, 1991