Medline recalls two kits with Olympus biopsy valves due to reported rubber fragments detaching, potentially causing airway blockage or requiring removal. Affected kits include specific model numbers and batch codes.
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 two types of biopsy kits that contain Olympus biopsy valves. These kits risk releasing small rubber pieces that could get stuck in a patient's airway, requiring medical intervention.
Rubber fragments inside the biopsy valves can detach during use. If these fragments enter the patient's airway, they may cause breathing difficulties, require removal, or lead to inflammation and oxygen shortage.
Healthcare professionals using Medline's Olympus biopsy kits are most at risk. Patients undergoing procedures with these kits could face airway blockage or complications.
Check if your kit has model numbers DYNDA2137B (BAL KIT) or DYKE1915 (ENDO KIT). Look for batch codes listed in the recall notice, such as 24DBW065 through 26ABE643.
Identify if your kit matches the model numbers DYNDA2137B or DYKE1915 listed in the recall.
Reach out to Medline directly for guidance on whether your kit is affected and next steps.
Olympus is investigating an increase in complaints about rubber fragments detaching from the biopsy valves, which could cause airway blockage or require medical intervention.
Check if your kit matches the model numbers DYNDA2137B or DYKE1915 and contact Medline for specific instructions.
Yes, if rubber fragments enter the airway, patients may need medical intervention for removal, which could cause breathing difficulties or inflammation.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1708-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1708-2026 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.
