Devices

Device Recall Deltec PortACath

Model / Serial
Lot M27037
Distribution
The recalled products were shipped nationwide in the United States and worldwide.
Product Description
Port-A-Cath II Epidural Low Profile Polysulfone/Titanium Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 5mm I.D., REF 21-1501-22
Manufacturer
Deltec, Inc
1 Event
- Recall of Device Recall Deltec PortACath

Manufacturer

Deltec, Inc

Manufacturer Address
Deltec, Inc, 1265 Grey Fox Rd, Saint Paul MN 55112-6929
Source
USFDA

18 devices with a similar name

Learn more about the data here

Device Recall Deltec PortACath

Model / Serial
Lot M27052
Product Classification
General Hospital and Personal Use Devices
Device Class
3
Implanted device?
No
Distribution
The recalled products were shipped nationwide in the United States and worldwide.
Product Description
Port-A-Cath II Low Profile Epidural Implantable Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 0.5mm I.D., REF 21-1501-01
Manufacturer
Deltec, Inc

Device Recall Deltec PortACath

Model / Serial
Lot M27134
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 Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr Introducer Set, REF 21-4009-24
Manufacturer
Deltec, Inc

Device Recall Deltec PortACath

Model / Serial
Lot M27051
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 Low Profile Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr Introducer Set, REF 21-4035-24
Manufacturer
Deltec, Inc

Device Recall Deltec PortACath

Model / Serial
Lots M27118 and M27262
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 Low Profile Titanium Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 Fr Introducer Set, REF 21-4037-24
Manufacturer
Deltec, Inc

Device Recall Deltec PortACath

Model / Serial
Lot M26890
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
The recalled products were shipped nationwide in the United States and worldwide.
Product Description
6 Fr Introducer Set, REF 21-2320-24
Manufacturer
Deltec, Inc

13 more

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

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.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)