Class II — Potential Health Hazard

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

FIRMap" Catheter Recalled by Abbott Due to Incorrect product labeling.

Date: April 28, 2022
Company: Abbott
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 Abbott directly.

Affected Products

FIRMap" Catheter, 60mm Basket

Quantity: 40 units

Why Was This Recalled?

Incorrect product labeling.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Abbott

Abbott has 19 total recalls tracked by RecallDetector.

Related Recalls

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