Medline recalls specific Olympus biopsy valve kits after reports of rubber fragments detaching, potentially causing airway blockages or requiring 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 certain Olympus biopsy valve kits because rubber fragments may detach during use, leading to foreign bodies in the airway that could require removal. This poses a risk of serious complications like inflammation or breathing difficulties.
The biopsy valves contain rubber that can detach, creating small fragments that may enter the airway. This could cause blockages, inflammation, or breathing problems requiring medical intervention.
Healthcare professionals using the recalled Olympus biopsy valves for bronchoscopy procedures are most at risk. Patients undergoing these procedures with the affected kits could experience airway blockages.
Check for kits labeled with model numbers: DYNJ900898I, DYNJ901922G, DYKM1417I, DYKM1417J, DYNJ58146A, or DYNDA2138A. These were sold with specific lot numbers from 2024 to 2025.
Identify the model numbers on the kit packaging to confirm if it matches the recalled items listed in the notice.
Reach out to Medline directly to request a replacement kit or return the affected product for a new one.
The recalled models include DYNJ900898I, DYNJ901922G, DYKM1417I, DYKM1417J, DYNJ58146A, and DYNDA2138A.
The recall does not specify that the kits must be stopped immediately; however, it is recommended to check for the specific model numbers and contact Medline for a replacement.
Rubber fragments may detach, leading to foreign bodies in the airway, which could cause inflammation, breathing difficulties, or require medical intervention.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1709-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1709-2026 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.
