Boston Scientific Corporation Titanium Dual Lumen Implantable Port with PASV Valve and 10F Silicone Catheter. Catalog No/REF: PRTB10A, Model No. M001PRTB10A. Firm on label: Boston Scientific Corp., NAMIC Technology Center, Glens Falls, NY 12801. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Titanium Dual Lumen Implantable Port with PASV Valve and 10F Silicone Catheter. Catalog No/REF: PRTB10A, Model No. M001PRTB10A. Firm on label: Boston Scientific Corp., NAMIC Technology Center, Glens Falls, NY 12801.
Brand
Boston Scientific Corporation
Lot Codes / Batch Numbers
916252, 917973
Products Sold
916252, 917973
Boston Scientific Corporation is recalling Titanium Dual Lumen Implantable Port with PASV Valve and 10F Silicone Catheter. Catalog No/REF: PRT due to Catheters may not have adequate radiopacity for proper visualization under fluoroscopy.. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: distribution information.
Reason for Recall
As stated by FDA
Catheters may not have adequate radiopacity for proper visualization under fluoroscopy.
Recommended Action
Per FDA guidance
Letters dated 3/29/04 with instruction to remove and return product.
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