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Manufacturers
Deltec, Inc
Manufacturer Address
Deltec, Inc, 1265 Grey Fox Rd, Saint Paul MN 55112-6929
Source
USFDA
23 Events
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec PortACath
Recall of Device Recall Deltec ProPort
Recall of Device Recall Deltec ProPort
Recall of Device Recall Deltec ProPort
Recall of Device Recall Deltec ProPort
Recall of Device Recall Deltec PortACath P.A.S. Port
Recall of Device Recall Deltec PortACath II FluoroFree
Recall of Device Recall Deltec PortACath II
Recall of Device Recall Deltec PortACath II
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23 devices in the database
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
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
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
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
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
18 more
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Deltec, Inc
Manufacturer Address
Deltec, Inc, 1265 Grey Fox Road, St Paul MN 55112
Source
USFDA
Language
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