Medline recalls Thoracic Robots DYNJ908777B due to potential rubber fragments detaching from biopsy valves, risking airway obstruction and medical intervention.
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.
Medline is recalling Thoracic Robots with specific model numbers because their biopsy valves may detach rubber fragments that could enter the patient's airway. This poses a risk of requiring medical intervention to remove the fragments.
The biopsy valves in the Thoracic Robots may detach rubber fragments during use. These fragments can enter the patient's airway, potentially causing blockages that require medical removal, inflammation, low oxygen levels, or longer procedure times.
Healthcare professionals using the Thoracic Robots devices for procedures involving biopsy valves. Patients undergoing procedures with these devices are at risk if fragments enter the airway.
Check for the model number DYNJ908777B on the device. The product was sold with specific lot numbers including 25EBD732, 25GBG733, 25IBQ613, 25JBD457, 25KBT352, 26ABA235, and 26ABP735.
Verify the model number on the device to confirm if it matches DYNJ908777B.
Reach out to Medline Industries for guidance on next steps if the device is affected.
Olympus is investigating an increase in complaints about rubber fragments detaching from biopsy valves, which could enter the patient's airway.
It may require medical intervention to remove the fragments, causing inflammation, low oxygen levels, or longer procedure times.
Check for the model number DYNJ908777B and lot numbers including 25EBD732, 25GBG733, 25IBQ613, 25JBD457, 25KBT352, 26ABA235, or 26ABP735.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1707-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1707-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
