POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1668362
Reported: May 16, 2018 Initiated: February 8, 2018 #Z-1761-2018
Product Description
POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1668362
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
- 2395 units
- Distribution
- Nationwide
- Location
- Tempe, AZ
Frequently Asked Questions
What product was recalled? ▼
POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1668362. Recalled by Bard Peripheral Vascular Inc. Units affected: 2395 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-1761-2018.
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