Arrow International Inc: Medical Device Recall in 2017 - (Recall #: Z-1705-2017)

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:

The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein.

Product Classification:

Class II

Date Initiated: March 3, 2017

Date Posted: April 12, 2017

Recall Number: Z-1705-2017

Event ID: 76637

Reason for Recall:

Arrow International, Inc. notified its customers who received the affected Antimicrobial/Antithrombogenic PICC Kits, that the kits were being recalled due to a labeling error. The lidstock on some of the kits reads CDC-45541-HPK1A, while the banner card on the side of the kit reads CDC-45052-HPK1A. Other kits may list CDC-45052-HPK1A on the lidstock and CDC-45541-HPK1A on the banner card. The affected lot numbers are 23F16C0851, 23F16A0727, and 23F16C0844.

Status: Terminated

Product Quantity: 1,351 catheters

Code Information:

Device Listing Number: D149129 Lot Numbers: 23F16C0851, 23F16A0727 and 23F16C0844

Distribution Pattern:

US Distribution

Voluntary or Mandated:

Voluntary: Firm initiated