Medline Industries, LP

Devices recall · Z-1707-2026

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.

Product description

THORACIC ROBOTS, DYNJ908777B

Recalling firm

Medline Industries, LP

Product quantity

14,379 kits total

Lot / code info

UDI-DI 10198459269196 (EA) 40198459269197 (CS) LOTS 25EBD732 25GBG733 25IBQ613 25JBD457 25KBT352 26ABA235 26ABP735

Distribution

US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.

Recall initiated

2026-02-16

Status

Ongoing

Location

Northfield, IL, United States

Voluntary / mandated

Voluntary: Firm initiated

Data from official federal safety records. Updated periodically. Verify on FDA.gov