Medline recalls Airway Exam Kit DYKE1796 due to potential rubber fragments detaching from biopsy valves, risking airway blockage 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 Airway Exam Kit DYKE179:6 because it contains Olympus biopsy valves that may detach rubber fragments. This could cause foreign objects to enter the airway, requiring medical removal or causing breathing issues.
Rubber fragments from the biopsy valves may detach during use, entering the airway. This can cause blockages, inflammation, low oxygen levels, or require emergency medical intervention to remove the fragments.
Healthcare professionals using the Airway Exam Kit for procedures are most at risk. Patients undergoing airway exams with this kit could experience breathing problems.
Check for the model number DYKE1796 on the kit. The kit was sold with specific lot numbers: 24CBT023, 24FBB701, 24LBL343, and 25GBP141.
Verify the model number DYKE1796 and lot numbers 24CBT023, 24FBB701, 24LBL343, or 25GBP141.
Olympus is investigating increased complaints of rubber fragments detaching from biopsy valves, which could cause airway blockages or require medical intervention.
Check the model number and lot numbers to confirm if it's recalled. Contact Medline for further instructions.
Yes, if fragments enter the airway, it may require emergency medical removal or cause breathing problems.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1705-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1705-2026 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.
