Arrow International Inc: Medical Device Recall in 2017 - (Recall #: Z-2170-2017)

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:

Arrow(R) VPS(R) Access Kit for use with 4 and 5 Fr. Peripherally Inserted Central Venous Catheters

Product Classification:

Class II

Date Initiated: April 28, 2017

Date Posted: June 7, 2017

Recall Number: Z-2170-2017

Event ID: 77163

Reason for Recall:

Arrow International is notifying each customer who received the affected that product that the kits do not contain important information regarding the 3M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing.

Status: Terminated

Product Quantity: 3,918 units

Code Information:

ASK-04001-DU9 and ASK-04001-DU10 Device Listing Number D156491 Lot Numbers: 23F15L0593 23F16A0300 23F16B0028 23F16B0523 23F16J0151 23F16K0363 23F16K0431 23F16K0820 23F15L0662 23F16A0298 23F16B0338 23F16C0321 23F16C0632 23F16J0105 23F16K0449

Distribution Pattern:

US Distribution to the state of : NC

Voluntary or Mandated:

Voluntary: Firm initiated