Integra LifeSciences Corp. recalled 55,276 units of MEDIHONEY Calcium Alginate with Active Leptospermum Honey on January 16, 2026. The recall cites potential packaging failures that may compromise sterility. Affected products include model numbers 31012, 31022, and 31045.
Potential packaging failures, which could lead to a breach in the sterile barrier.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Integra LifeSciences Corp. (NeuroSciences) or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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MEDIHONEY Calcium Alginate is used for managing moderately to heavily exuding wounds. It aids in autolytic debridement and is sought after for its wound healing properties due to the presence of Active Leptospermum Honey.
The recall is due to potential failures in the packaging that could allow germs to enter and compromise the product's sterility. This could lead to infections if used on wounds.
This recall is not part of a broader industry pattern.
The recall prompts immediate action for users, as using a compromised product could lead to serious health risks, especially for vulnerable individuals with wounds.
Model numbers and lot numbers can be found on the product packaging or the accompanying documentation.
Expect a refund or replacement to take about 4-8 weeks after contacting the manufacturer.
Keep a record of your purchase receipt, any communications with the company, and photographs of the product.
This recall involves MEDIHONEY Calcium Alginate with Active Leptospermum Honey, model numbers 31012, 31022, and 31045. The products were distributed worldwide, including across multiple U.S. states such as Texas, Michigan, and Florida. The exact quantity recalled is 55,276 units.
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