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Medium risk Drugs & MedicationsClass II

Medline Industries, LP Recall

THORACIC ROBOTS, DYNJ908777B

Updated February 16, 2026

Medline Industries, LP is recalling THORACIC ROBOTS, DYNJ908777B. 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.

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

What is recalled

THORACIC ROBOTS, DYNJ908777B

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

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
Drugs & Medications
Recall ID
fda-Z-1707-2026
Classification
Class II
Recalled
February 16, 2026
Read the official notice

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