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Devices
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
Manufacturer
Deltec, Inc
1 Event
Recall of Device Recall Deltec ProPort
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Manufacturer
Deltec, Inc
Manufacturer Address
Deltec, Inc, 1265 Grey Fox Rd, Saint Paul MN 55112-6929
Source
USFDA
3 devices with a similar name
Learn more about the data
here
Device Recall Deltec ProPort
Model / Serial
Lot M27054
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 Plastic Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., 8.5 French Introducer Set, REF 21-4155-24
Manufacturer
Deltec, Inc
Device Recall Deltec ProPort
Model / Serial
Lot M27136
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 Plastic Venous Access System, Pre-assembled with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., 8.5 French Introducer Set, REF 21-4165-24
Manufacturer
Deltec, Inc
Device Recall Deltec ProPort
Model / Serial
Lot M27046
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, 2.6mm O.D. x 1.6mm I.D., 8.5 French Introducer Set, REF 21-4171-24
Manufacturer
Deltec, Inc
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