Quick Facts at a Glance
- Recall Date
- January 16, 2026
- Hazard Level
- HIGH
- Brand
- Integra LifeSciences Corp.
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Integra LifeSciences Corp.
- Product type
- Calcium Alginate Dressing
- Model numbers
- (1) Model Number: 31012, UDI-DI: 10381780486909, Lot numbers: A24008, A24057, B21123, B24075, C22159, C23177 +12 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 16, 2026
Reported by FDA DEVICE
February 25, 2026
RecallRadar source check
March 4, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Potential packaging failures, which could lead to a breach in the sterile barrier.
What You Should Do
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
About This Product
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.
Why This Is Dangerous
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.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall prompts immediate action for users, as using a compromised product could lead to serious health risks, especially for vulnerable individuals with wounds.
Practical Guidance
How to identify if yours is affected
- Check the model number on the packaging.
- Look for lot numbers: A24008, A24057, B21123, etc.
- Confirm if the product was purchased during the recall period.
Where to find product info
Model numbers and lot numbers can be found on the product packaging or the accompanying documentation.
What timeline to expect
Expect a refund or replacement to take about 4-8 weeks after contacting the manufacturer.
If the manufacturer is unresponsive
- Document all communications with the company.
- Consider reaching out via different contact methods if no response is received.
How to prevent similar issues
- Always check for recall notices before purchasing medical devices.
- Look for certifications indicating quality control and sterility.
Documentation advice
Keep a record of your purchase receipt, any communications with the company, and photographs of the product.
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Product Details
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.
Key Facts
- Recall date: January 16, 2026
- Reported date: February 25, 2026
- Quantity recalled: 55,276 units
- Affected model numbers: 31012, 31022, 31045
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Safety Guide
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