FDA Enforcement Class II Terminated

Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The ArrowEVOLUTIONTM Pressure injectable P1CC with chlorag+ard Antimicrobial and Antithrombogenic Technology is indicated for short-term or long-term peripheral access to the central venous system for intravenous therapy, blood sampling, infusion, pressure injection of contrast media, and allows for central venous pressure monitoring

Recall: Z-2262-2017 · Reported June 14, 2017

Enforcement

Recall Number
Z-2262-2017
Event ID
76937
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Arrow International Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
June 14, 2017
Initiation Date
March 20, 2017
Classification Date
June 6, 2017
Termination Date
December 18, 2018
Address
2400 Bernville Rd, N/A, Reading, PA, 19605-9607, United States

Description

Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The ArrowEVOLUTIONTM Pressure injectable P1CC with chlorag+ard Antimicrobial and Antithrombogenic Technology is indicated for short-term or long-term peripheral access to the central venous system for intravenous therapy, blood sampling, infusion, pressure injection of contrast media, and allows for central venous pressure monitoring

Reason

Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.

Code Info

Material Number ASK-45552-SPH

Distribution

Nationwide Distribution

Quantity

43,394 units