VISARIS DOO

US Last updated 31 May 2026 Part of Visaris D.O.O.

Catalogue0

No devices listed yet from this manufacturer.

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

2018
- 5 Apr 2018 Z-1880-2018 Class II Terminated A failure of the tube arm suspension is possible while the tube arm height is being adjusted. During tube height adjustment there is a small probability of failure of both the primary and redundant holding mechanisms, causing uncontrollable descent of the tube arm and a potential risk of injury to the patient.
- 5 Apr 2018 Z-1881-2018 Class II Terminated A failure of the tube arm suspension is possible while the tube arm height is being adjusted. During tube height adjustment there is a small probability of failure of both the primary and redundant holding mechanisms, causing uncontrollable descent of the tube arm and a potential risk of injury to the patient.
- 5 Apr 2018 Z-1882-2018 Class II Terminated A failure of the tube arm suspension is possible while the tube arm height is being adjusted. During tube height adjustment there is a small probability of failure of both the primary and redundant holding mechanisms, causing uncontrollable descent of the tube arm and a potential risk of injury to the patient.

Registered with the FDA under this company group, matched by name.