← FDA ENFORCEMENT
Z-0460-2026Class II

Sonesta Medical AB

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Sonesta Medical AB
Product type
Device
Status
Ongoing
Report date
2025-11-19
Distribution
US Distribution to NH only.
Product quantity
10 tables
Initiated by
Voluntary: Firm initiated
Reason for recall

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

Product description

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

Code / lot info

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

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →