POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with open suture holes, REF 5678301
Reported: May 16, 2018 Initiated: February 8, 2018 #Z-1771-2018
Product Description
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with open suture holes, REF 5678301
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
- 181 units
- Distribution
- Nationwide
- Location
- Tempe, AZ
Frequently Asked Questions
What product was recalled? ▼
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with open suture holes, REF 5678301. Recalled by Bard Peripheral Vascular Inc. Units affected: 181 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-1771-2018.
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