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Medline Thoracic Robot DYNJ908777B Recall

THORACIC ROBOTS, DYNJ908777B

Updated February 16, 2026

Medline thoracic robot kits contain recalled Olympus biopsy valves that may shed rubber fragments. These fragments can lodge in the airway and require surgical removal, or trigger inflammation and low oxygen levels.

Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on February 16, 2026. Details below.

What is recalled

Thoracic Robots, model DYNJ908777B, manufactured by Medline Industries, LP. Specifically, the kits contain recalled Olympus single-use biopsy valves.

Am I affected

You're affected if you are a healthcare facility that received Thoracic Robot kits, model DYNJ908777B, from Medline Industries that contain Olympus biopsy valves.

What to do right now

Stop using the recalled Olympus biopsy valves in these kits immediately. Contact Medline Industries, LP to arrange return or replacement of the affected valves.

The hazard

Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.

Brands affected

Medline Industries, LP
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1707-2026
Classification
Class II
Recalled
February 16, 2026
Read the official notice

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