Arrow International Inc: Medical Device Recall in 2021 - (Recall #: Z-2071-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Arrow Temporary Pacing Catheter/Introducer Kit 5Fr. pacing catheter 6 Fr. introducer Product Code: AI-07155-IK - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.

Product Classification:

Class II

Date Initiated: May 19, 2021

Date Posted: July 21, 2021

Recall Number: Z-2071-2021

Event ID: 88120

Reason for Recall:

Marketed without a 510K

Status: Ongoing

Product Quantity: 15 units

Code Information:

Lot Numbers: 23F20A0230 23F20E0004 23F20E0094

Distribution Pattern:

US Nationwide distribution in the states of FL, ID, IL, NY, OH, TX.

Voluntary or Mandated:

Voluntary: Firm initiated