Arrow International Inc Arrow Double-Lumen Balloon Wedge Pressure Catheter, for sampling blood for oxygen levels and measuring pressures in the right heart. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Arrow Double-Lumen Balloon Wedge Pressure Catheter, for sampling blood for oxygen levels and measuring pressures in the right heart.
Brand
Arrow International Inc
Lot Codes / Batch Numbers
MF5124329
Products Sold
MF5124329
Arrow International Inc is recalling Arrow Double-Lumen Balloon Wedge Pressure Catheter, for sampling blood for oxygen levels and measuri due to The print identifying the two extension lines, CVP Proximal and PA Distal, are reversed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The print identifying the two extension lines, CVP Proximal and PA Distal, are reversed.
Recommended Action
Per FDA guidance
Recall letter was sent to customers on 6/20/2006 by US mail.
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 noticeDistribution
As reported by FDA
IL, IN, MD, MA, MO
Page updated: Jan 10, 2026