Integra LifeSciences recalls MediHoney tubes (models 31515, 31535) due to packaging failures that could breach sterile barrier. Affected units include specific lot numbers. Consumers should check packaging for recall details.
Packaging failures were identified which could lead to a breach in the sterile barrier.
Integra LifeSciences is recalling MediHoney wound care tubes with model numbers 31515 and 31535 because packaging failures might break the sterile barrier. This could expose wounds to infection during use.
The packaging may fail, breaking the sterile barrier that protects wounds from infection. This could allow bacteria to enter the wound site if the tube is used without proper protection.
People using MediHoney tubes for wound care are affected. Those with open wounds or recent injuries are at slightly higher risk due to potential infection.
Check for model numbers 31515 or 31535 on the MediHoney tube packaging. Affected units have specific lot numbers listed in the recall notice.
Look for model numbers 31515 or 31535 on the MediHoney tube packaging.
Packaging failures could lead to a breach in the sterile barrier, potentially exposing wounds to infection.
Model numbers 31515 and 31535.
Check the packaging for model numbers 31515 or 31535 and specific lot numbers listed in the recall notice.
We’ve drafted a message you can send MediHoney to request your refund or repair — edit it as you like.
Subject: Recall Z-2506-2025 — MediHoney MediHoney Hello, I own a MediHoney that is covered by recall Z-2506-2025 from MediHoney. 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.
