Arrow International Inc Implantable Vascular Access System -- Infusion Ports with Silicone Rubber catheter. Latex Free A Port Ref Product No. AP-01007. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Implantable Vascular Access System -- Infusion Ports with Silicone Rubber catheter. Latex Free A Port Ref Product No. AP-01007.
Brand
Arrow International Inc
Lot Codes / Batch Numbers
Product code AP-01007: MF2041118, MF2112625, MF3013201, MF3105944, MF4031465.
Products Sold
Product code AP-01007: MF2041118, MF2112625, MF3013201, MF3105944, MF4031465.
Arrow International Inc is recalling Implantable Vascular Access System -- Infusion Ports with Silicone Rubber catheter. Latex Free A due to Catheter has separated from the infusion port body.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Catheter has separated from the infusion port body.
Recommended Action
Per FDA guidance
The recall notification was sent out to their US customers on 9/29/2006.
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