Arrow International Inc: Medical Device Recall in 2018 - (Recall #: Z-0601-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

ARROW PICC powered by ARROW VPS Stylet, Product Codes: CDC-35052-VPS and CDC-35041-VPS. Peripherally Inserted Central Catheter

Product Classification:

Class II

Date Initiated: July 25, 2017

Date Posted: February 21, 2018

Recall Number: Z-0601-2018

Event ID: 78964

Reason for Recall:

Finished good kits may contain incorrect components. Kits that should contain a 5 FR 2 lumen catheter may contain a 4 FR single lumen catheter and kits that should contain a 4 FR single lumen catheter may contain a 5 FR 2 lumen catheter. This may cause a delay in treatment while a replacement catheter is obtained.

Status: Terminated

Product Quantity: 2691 total

Code Information:

Lot/Batch Numbers: 23F17A0038, 23F17A0040, 23F16M0059.

Distribution Pattern:

US nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated