Arrow International Inc: Medical Device Recall in 2020 - (Recall #: Z-1238-2020)

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 FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN

Product Classification:

Class II

Date Initiated: December 20, 2019

Date Posted: February 26, 2020

Recall Number: Z-1238-2020

Event ID: 84688

Reason for Recall:

Product lidstock contains the incorrect expiration date for the product

Status: Terminated

Product Quantity: 205

Code Information:

Lot Number: 13F18K0740

Distribution Pattern:

Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA

Voluntary or Mandated:

Voluntary: Firm initiated