Integra LifeSciences recalls MediHoney Paste 31505 due to potential sterile packaging breaches. This could compromise wound healing. Affected units include specific lot numbers.
Packaging failures were identified which could lead to a breach in the sterile barrier.
Integra LifeSciences recalls MediHoney Paste 31505 because its packaging might fail, risking contamination of the sterile wound dressing. This could lead to infection or delayed healing if the dressing is not properly protected.
The packaging could breach the sterile barrier, allowing bacteria or contaminants to enter the wound dressing. This might compromise the dressing's ability to heal wounds properly and increase infection risk.
Patients using MediHoney Paste 31505 for wound care are affected. Those with open wounds or recent injuries are at higher risk due to potential contamination.
Check for the model number 31505 on the MediHoney Paste packaging. Affected units include specific lot numbers: 2150, 2336, 2151, 2337, 2201, 2414, 2209, 2415, 2217, 2417, 2232, 2428, 2241, 2434, 2301, 2435, 2312, 2505, 2313, 2508, 2314, 2509, 2328.
Inspect the MediHoney Paste packaging for the model number 31505 and affected lot numbers.
The recall indicates potential packaging failures that could compromise sterility, so it is not recommended for use until the remedy is applied.
Check the lot number on the packaging. If it matches the affected lots listed, stop using it and contact Integra LifeSciences for instructions.
Look for the model number 31505 and check the lot number against the list of affected lots provided 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-2505-2025 — MediHoney MediHoney Hello, I own a MediHoney that is covered by recall Z-2505-2025 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.
