United StatesThe Sonesta 6210 procedure table (Brand Sonesta, Model/Catalog 0120-LA120-03; Primary DI 07350006950018; serial numbers 12-70791 through 12-70801) used for full fluoroscopic imaging during video urodynamics is subject to recall; 10 tables were distributed in the US to NH only. It was recalled because the table may contain an inadequate weld on the backrest bracket, which can result in the backrest dropping.
What's being recalled
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
Recalling firm: Sonesta Medical AB, Solna, Sweden.
How to identify it
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
The hazard
Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Distribution to NH only.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)