Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC Recalled by Arrow International Inc Due to Product lidstock contains the incorrect expiration date for...

Date: December 20, 2019
Company: Arrow International Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Arrow International Inc directly.

Affected Products

Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC

Why Was This Recalled?

Product lidstock contains the incorrect expiration date for the product

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Arrow International Inc

Arrow International Inc has 431 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report