Devices

Device Recall POWERPORT(R) ClearVUE(R) Slim with Smooth Septum, 8F Polyurethane Catheter with Open Suture Holes

Model / Serial
Lot Number Unique Device Identifier (UDI) REAN0067 (01)00801741110825(17)170628(10)REAN0067 REAP0630 (01)00801741110825(17)170728(10)REAP0630 REAS2309 (01)00801741110825(17)171028(10)REAS2309 REAV2088 (01)00801741110825(17)171028(10)REAV2088 REAY0330 (01)00801741110825(17)171031(10)REAY0330 REBS1275 (01)00801741110825(17)180731(10)REBS1275 REBT1568 (01)00801741110825(17)181031(10)REBT1568 REBV0713 (01)00801741110825(17)181231(10)REBV0713
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide
Product Description
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1678301
Manufacturer
Bard Peripheral Vascular Inc
1 Event
- Recall of Device Recall POWERPORT(R) ClearVUE(R) Slim with Smooth Septum, 8F Polyurethane Catheter with Open Suture Holes

Manufacturer

Bard Peripheral Vascular Inc

Manufacturer Address
Bard Peripheral Vascular Inc, 1625 W 3rd St Bldg 1, Tempe AZ 85281-2438
Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
USFDA

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