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Medline Industries, LP recalls THORACIC ROBOTS, DYNJ908777B

Recalled April 8, 2026 · FDA recall Z-1707-2026 · Medline Industries

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. · FDA Class II
Units
14,379 kits total
Sold at
US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.

Description

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.

Product
THORACIC ROBOTS, DYNJ908777B
Manufacturer(s)
Medline Industries, LP

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Medline Industries, LP recalls THORACIC ROBOTS, DYNJ908777B | RecallWatchUSA