ClearanceBrief
Recall Z-1501-2009 ยท MCW Catheter, Peripheral, Atherectomy

Arrow International Inc

Arrow Percutaneous Thrombolytic Device (PTD) for fistula and dialysis grafts

DateJun 24, 2009 (initiated Feb 11, 2009)
StatusTerminated
ReasonLeakage: Material not lipid resistant, may crack and/or leak. Use of this device with lipid containing solutions or 70% isopropyl alcohol may cause leakage or air embolism.
Root causeDevice Design
ActionArrow International issued a letter dated 2/18/09 to all customers informing them of the problem and if a lipid resistant stopcock is required to contact the firm for replacements. New labels state: Warning - do not use with lipid containing solutions or 70% isopropyl alcohol, as these solutions may cause leakage or air embolism.
Quantity900,000 total, all products
DistributionWorldwide distribution: USA, Argentina, Australia, Bahamas, Belarus, Belgium, Brazil, Chile, China, Colombia, Costa Rica, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Finland, France, Germany, Greece, Guatemala, Hungary, Iceland, India, Indonesia, Ireland, Israel, Italy, Japan, Lat
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K990829ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD, MODELS PT-45509 (CATHETER KIT WITH INTRODUCER SHEATHS),PT-65
Arrow Intl., Inc., May 4, 1999