POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00005
Reported: May 16, 2018 Initiated: February 8, 2018 #Z-1773-2018
Product Description
POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00005
Reason for Recall
The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
Details
- Recalling Firm
- Bard Peripheral Vascular Inc
- Units Affected
- 10 units
- Distribution
- Nationwide
- Location
- Tempe, AZ
Frequently Asked Questions
What product was recalled? ▼
POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00005. Recalled by Bard Peripheral Vascular Inc. Units affected: 10 units.
Why was this product recalled? ▼
The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 16, 2018. Severity: Moderate. Recall number: Z-1773-2018.
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