Medline recalls Anterior Hip Pack DYNJ64672B due to potential rubber fragments detaching from biopsy valves, risking foreign body in airways. Affected units have specific UDI-DI and lot numbers.
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 Anterior Hip Packs with model DYNJ6462B because rubber fragments from the biopsy valves might detach and enter the airways, requiring medical intervention. This risk is serious but only affects specific units with known UDI-DI and lot numbers.
Rubber fragments can detach from the biopsy valves during use, potentially entering the airways. This may cause serious complications like airway blockage, inflammation, or the need for emergency medical procedures.
Patients using the recalled Anterior Hip Packs for surgery are most at risk. The recall applies to specific units with UDI-DI numbers 10195327377496 (EA) and 40195327377497 (CS) from lot 23LMD300.
Check for the model number DYNJ64672B on the Anterior Hip Pack. Affected units have UDI-DI numbers 10195327377496 (EA) or 40195327377497 (CS) and lot number 23LMD300.
Immediately stop using the recalled Anterior Hip Pack if it has the model number DYNJ64672B and the specified UDI-DI and lot numbers.
The recalled product is the Medline Anterior Hip Pack with model number DYNJ64672B.
Detached fragments could enter the airways, potentially requiring medical intervention such as removal procedures.
Check for the model number DYNJ64672B and UDI-DI numbers 10195327377496 (EA) or 40195327377497 (CS) with lot number 23LMD300.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1711-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1711-2026 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.
