Class II — Potential Health Hazard

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

BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended Recalled by Verathon, Inc. Due to Due to a change in handle material and...

Date: September 29, 2020
Company: Verathon, 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 Verathon, Inc. directly.

Affected Products

BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the bladder noninvasively.

Quantity: 398 units

Why Was This Recalled?

Due to a change in handle material and process, probe handle may crack.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Verathon, Inc.

Verathon, Inc. has 13 total recalls tracked by RecallDetector.

Related Recalls

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