Class II — Potential Health Hazard

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

Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software Recalled by Sonesta Medical AB Due to Video fluoroscopy table may contain inadequate weld on...

Date: August 22, 2025
Company: Sonesta Medical AB
Status: Ongoing
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 Sonesta Medical AB directly.

Affected Products

Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software Version: N/A Product Description: Sonesta 6210 - Procedure table designed for full fluoroscopic imaging of the urinary tract during video Urodynamics procedures. Component: N/A

Quantity: 10 tables

Why Was This Recalled?

Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.

Where Was This Sold?

This product was distributed to 1 state: NH

Affected (1 state)Not affected

About Sonesta Medical AB

Sonesta Medical AB has 1 total recall tracked by RecallDetector.

Related Recalls

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