HIGH

Integra LifeSciences Recalls Medical Dressing Due to Sterility Risk

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.

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

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

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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.

The Hazard

The recall is due to potential packaging failures which could lead to a breach in the sterile barrier. This defect poses a high risk of infection for patients using the products for wound management.

Reported Incidents

There are no specific reports of injuries or incidents linked to this recall. The nature of the recall indicates a preventative measure against potential health risks.

What to Do

Patients and healthcare providers should stop using the affected products immediately. They should follow the recall instructions provided by Integra LifeSciences Corp. for further guidance.

Contact Information

For further information, contact Integra LifeSciences Corp. at their designated customer service lines or through their website. The recall notification may be communicated through email, fax, letter, press releases, or phone calls.

Key Facts

  • Recall date: January 16, 2026
  • Reported date: February 25, 2026
  • Quantity recalled: 55,276 units
  • Affected model numbers: 31012, 31022, 31045
  • Distribution: Worldwide

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
(1) Model Number: 31012
UDI-DI: 10381780486909
Lot numbers: A24008
A24057
B21123
+15 more
Affected States
ALL
Report Date
February 25, 2026
Recall Status
ACTIVE

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