International Medical Devices Database

23 devices in the database

Device Recall Deltec PortACath II

Model / Serial
Lot M26983
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
Yes
Distribution
The recalled products were shipped nationwide in the United States and worldwide.
Product Description
Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen PolyFlow Polyurethane Catheter, 3.2mm O.D. x 1.4mm I.D., 10 French Introducer Set, REF 21-8068-24

Device Recall Deltec PortACath II

Model / Serial
Lots M26975 and M27127
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
Yes
Distribution
The recalled products were shipped nationwide in the United States and worldwide.
Product Description
Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen PolyFlow Polyurethane Catheter, 2.2mm O.D. x 1.0mm I.D., 7 French Introducer Set, REF 21-8066-24

Device Recall Deltec PortACath II FluoroFree

Model / Serial
Lot M27047
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
Yes
Distribution
The recalled products were shipped nationwide in the United States and worldwide.
Product Description
Port-A-Cath II Fluoro-Free Low Profile Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., and with CATH-FINDER Sensor Wire, REF 21-4685-24

Device Recall Deltec PortACath P.A.S. Port

Model / Serial
Lot M27049
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
Yes
Distribution
The recalled products were shipped nationwide in the United States and worldwide.
Product Description
Port-A-Cath P.A.S. Port T2 Titanium Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 French Introducer Set, REF 21-4573-24

Device Recall Deltec ProPort

Model / Serial
Lot M27048
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
Yes
Distribution
The recalled products were shipped nationwide in the United States and worldwide.
Product Description
ProPort Low Profile Plastic Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 French Introducer Set, REF 21-4183-24

18 more

One manufacturer with a similar name

Learn more about the data here

Deltec, Inc

Manufacturer Address
Deltec, Inc, 1265 Grey Fox Road, St Paul MN 55112
Source
USFDA

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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