UFSK recalls Treatment Chair 500 XLE models with serial numbers 2000-4506 due to potential seat drive failure during patient positioning, which could lead to unsafe chair movement.
Service life of the electrical seat part drive of the treatment chair may be shortened unexpectedly after several years of use due to a potential wear-related reduction in the self-locking of the drive and may remain undetected. A worsened self-locking of the seat drive can lead to overriding the drive s end position when positioning the patient with the seat part in an inclined position
UFSK is recalling Treatment Chair 500 XLE models with serial numbers 2000-4506 because the electrical seat drive may fail after years of use, risking patient injury if the chair moves unexpectedly while positioning. This could happen during diagnostic or therapeutic procedures where the chair is tilted.
The electrical seat drive may wear out over time, reducing its ability to lock securely. If the drive fails while the chair is tilted, it could move unexpectedly, potentially causing injury to the patient.
Healthcare providers using the chair for patient positioning during medical procedures are most at risk. Patients receiving treatments in ophthalmology or other specialties using this chair could be affected.
Check the serial number on the chair, which ranges from 2000 to 4506. The chair is used for diagnostic and therapeutic treatments, especially in ophthalmology.
Look for the serial number on the chair, which ranges from 2000 to 4506.
The electrical seat drive may wear out over time, reducing its ability to lock securely. If the drive fails while the chair is tilted, it could move unexpectedly, potentially causing injury to the patient.
Treatment Chair 500 XLE models with serial numbers 2000 to 4506.
Check the serial number on the chair; affected models have serial numbers from 2000 to 4506.
We’ve drafted a message you can send UFSK to request your refund or repair — edit it as you like.
Subject: Recall Z-2212-2023 — UFSK UFSK Hello, I own a UFSK that is covered by recall Z-2212-2023 from UFSK. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
