Sonesta Medical AB recalls Brand Name: Sonesta Product Name: 6210
- Recalling company
- Sonesta Medical AB
- 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 – may cause temporary or medically reversible health consequences
- Recall date
- Aug 22, 2025
- Reported
- Nov 19, 2025
- Distribution
- US Distribution to NH only.
- Status
- Ongoing
- Quantity
- 10 tables
- Lot / codes
- 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
- Company location
- Solna
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0460-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0460-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.