Arrow International Inc: Medical Device Recall in 2017 - (Recall #: Z-2292-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

"Pressure Injectable Jugular Axillo-Subclavian Central Catheter (JACC) Product" The CG+ Arrow JACC powered by Arrow VPS Stylet permits venous access to the central circulation through a central vein. The VPS Stylet, used with the VPS Console, quickly and accurately guides the central catheters to the desired location which is the lower third of the SVC or at the cavo-atrial junction

Product Classification:

Class II

Date Initiated: March 20, 2017

Date Posted: June 14, 2017

Recall Number: Z-2292-2017

Event ID: 76937

Reason for Recall:

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.

Status: Terminated

Product Quantity: unknown-firm reports total devices distributed 43,394

Code Information:

Material number CDC-41541-JX1A

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated