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Medium risk Medical DevicesClass II

MediHoney Gel Leptospermum Recall

MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with Active Leptospermum H

Updated January 16, 2026

MediHoney Gel with Active Leptospermum Honey wound dressings (models 31805 and 31815) are being recalled due to potential packaging failures that could compromise the sterile barrier. A breached sterile barrier increases the risk of infection when the dressing is applied to wounds.

Is the Integra LifeSciences Corp. (NeuroSciences) recalled? Yes. This product was recalled by FDA on January 16, 2026. Details below.

What is recalled

MediHoney Gel with Active Leptospermum Honey wound dressing. Model/Catalog Numbers: 31805 and 31815. Manufactured by Integra LifeSciences Corp.

Am I affected

You're affected if you have MediHoney Gel with Active Leptospermum Honey model 31805 or 31815 in your possession or facility.

What to do right now

Stop using this product immediately. Contact your healthcare provider or the facility where you obtained it for guidance on safe replacement wound dressings and proper disposal of the recalled units.

The hazard

Potential packaging failures, which could lead to a breach in the sterile barrier.

Brands affected

Integra LifeSciences Corp. (NeuroSciences)
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1363-2026
Classification
Class II
Recalled
January 16, 2026
Read the official notice

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