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
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-1363-2026
- Classification
- Class II
- Recalled
- January 16, 2026
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