Arrow International Inc: Medical Device Recall in 2017 - (Recall #: Z-2278-2017)

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:

AGB+ Pressure Injectable Multi-Lumen CVC Kit intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins

Product Classification:

Class II

Date Initiated: March 20, 2017

Date Posted: June 14, 2017

Recall Number: Z-2278-2017

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: N/A

Code Information:

Material number CA-42703-P1A

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated