Boston Scientific Corporation PASV Central Venous Catheter, 7F, Cat. # CVC702IK, Model # M0001CVC702IK. The 7Fr PASV Central Venous Catheter is a packaged configuration comprised of a silicone Central Venous Catheter with PASV Valve, Guidewire, Syringe, Needle, Tunneler, Scalpel, Sheath/Dilator, and caps. Firm on the label: Boston Scientific*** Manufactured at: 10 Glens Falls Technical Park, Glens Falls, NY 12801. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
PASV Central Venous Catheter, 7F, Cat. # CVC702IK, Model # M0001CVC702IK. The 7Fr PASV Central Venous Catheter is a packaged configuration comprised of a silicone Central Venous Catheter with PASV Valve, Guidewire, Syringe, Needle, Tunneler, Scalpel, Sheath/Dilator, and caps. Firm on the label: Boston Scientific*** Manufactured at: 10 Glens Falls Technical Park, Glens Falls, NY 12801.
Brand
Boston Scientific Corporation
Lot Codes / Batch Numbers
934445 exp. 2/28/2007, 942510 exp. 1/31/2007, 938122 exp. 3/31/2007, 935225 exp. 2/28/2007, 933703 exp 1/21/2007, 931401 exp. 12/31/2006, 929657 exp. 12/31/2006, 929435 exp. 12/31/2006.
Products Sold
934445 exp. 2/28/2007; 942510 exp. 1/31/2007; 938122 exp. 3/31/2007; 935225 exp. 2/28/2007; 933703 exp 1/21/2007; 931401 exp. 12/31/2006; 929657 exp. 12/31/2006; 929435 exp. 12/31/2006.
Boston Scientific Corporation is recalling PASV Central Venous Catheter, 7F, Cat. # CVC702IK, Model # M0001CVC702IK. The 7Fr PASV Central Ven due to Kits labeled to contain 0.028" guidewire contain 0.038" guidewire.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Kits labeled to contain 0.028" guidewire contain 0.038" guidewire.
Recommended Action
Per FDA guidance
Letters dated May 25, 2004 with instructions to return product to the Quincy, MA location.
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
IN
Page updated: Jan 10, 2026