Arrow International Inc: Medical Device Recall in 2020 - (Recall #: Z-0837-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH

Product Classification:

Class II

Date Initiated: December 6, 2019

Date Posted: January 29, 2020

Recall Number: Z-0837-2020

Event ID: 84520

Reason for Recall:

Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.

Status: Terminated

Product Quantity: 575

Code Information:

REF: ASK-00820-FLH Manufacturing Lots: 13F19E0247, 13F19F0006, and 13F19G0433 Exp. Date: Aug. 2020 - Sep. 2020

Distribution Pattern:

US: FL

Voluntary or Mandated:

Voluntary: Firm initiated