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Recall Category: Medical Device Recalls
Recalling Firm: Medline Industries, LP
Product: THORACIC ROBOTS, DYNJ908777B
Reason for Recall: 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.
Classification: Class II
Status: Ongoing
Report Date: 04/08/2026
Recall Initiation Date: 02/16/2026
Distribution: US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.
Code Info: UDI-DI 10198459269196 (EA) 40198459269197 (CS) LOTS 25EBD732 25GBG733 25IBQ613 25JBD457 25KBT352 26ABA235 26ABP735
Product Quantity: 14,379 kits total
Recall Type: Voluntary: Firm initiated
Firm Location: Northfield, IL, United States
Recall Number: Z-1707-2026
Event ID: 98530