Boston Scientific Corporation Tunneled Central Venous Catheters With PASV Valve Technology And Polyester Cuff - PASV CVC/DL/10/IK Catalog Number:CVC1002IK Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Tunneled Central Venous Catheters With PASV Valve Technology And Polyester Cuff - PASV CVC/DL/10/IK Catalog Number:CVC1002IK
Brand
Boston Scientific Corporation
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Lot Numbers: 976515 980606 987877 991181 995340 1009518 1010667 1012336 1015181 1018160 1019388 1022140 1026860 1029091
Boston Scientific Corporation is recalling Tunneled Central Venous Catheters With PASV Valve Technology And Polyester Cuff - PASV CVC/DL/10/IK due to The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.
Recommended Action
Per FDA guidance
Boston Scientific intiated the recall on 7/22/05 to direct accounts and to distributors on 7/ 27 /05. Distributors are requested to conduct sub recalls to the medical facility level. A revised letter dated 8/2/05 was sent to 18 US accounts for one lot (#1020895) omitted in the letter of 7/22/05.
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 noticePage updated: Jan 10, 2026