---
title: "Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 So... — FDA record Z-0460-2026 | Is It on Recall"
description: "Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping."
url: https://isitonrecall.com/recall/fda-device-z-0460-2026-brand-name-sonesta-product-name-6210-model-catalog-number-0120-la120-03-software-version-n-a-product/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software Version: N/A Product Description:... — FDA record Z-0460-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 22, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 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
- **Reason**: Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.
- **Classification**: Class II
- **Recalling firm**: Sonesta Medical AB
- **Quantity**: 10 tables
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0460-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0460-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot Code: Primary DI Number: 07350006950018 Serial numbers of potentially affected units: 12-70791 12-70792 12-70793 12-70794 12-70795 12-70796 12-70797 12-70798 12-70799 12-70801 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Distribution to NH only.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)

## Dates in the source

- **Report date**: Nov 19, 2025
- **Recall initiation date**: Aug 22, 2025
- **Center classification date**: Nov 7, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0460-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Sonesta Medical AB records](https://isitonrecall.com/brand/sonesta-medical-ab/)