Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Home Healthcare

MediHoney Wound Dressings Recalled for Packaging Failure and Sterility Risk

Agency Publication Date: February 13, 2026
Share:
Sign in to monitor this recall

Summary

Integra LifeSciences is recalling approximately 107,549 units of MediHoney wound care products, including MediHoney Gel, Calcium Alginate dressings, and Private Label CVS dressings. The recall was initiated due to potential packaging failures that could compromise the sterile barrier of the products. Using a non-sterile dressing on a wound can lead to serious infections. These products were distributed nationwide in the U.S. and internationally to various countries.

Risk

A breach in the sterile barrier of a wound dressing allows bacteria and other contaminants to enter the product. If these contaminated dressings are applied to light or heavily exuding wounds, it can cause localized or systemic infections in patients.

What You Should Do

  1. Check your MediHoney or CVS wound dressing packaging for the model numbers and lot/serial codes listed in the Affected Products section below.
  2. Stop using the recalled dressings immediately if they match any of the identified model numbers, serial numbers, or lot numbers.
  3. For healthcare professionals and clinical users, contact Integra LifeSciences Corp. or your distributor to arrange for the return, replacement, or correction of the affected devices.
  4. For consumers who purchased the private label CVS dressing, return the product to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or Integra LifeSciences for further instructions.
  5. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding medical device recalls.

Your Remedy Options

You have 3 options:

๐Ÿ“‹Option 1: Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
๐Ÿ’ฐOption 2: Full Refund
How to: For consumer products (CVS label), contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 3: Dispose of Product
How to: For consumer products (CVS label), stop using and throw the product away.

Affected Products

Product: MediHoney Gel with Active Leptospermum Honey
Model / REF:
31805
31815
Serial Numbers:
2405
2406
2407
2408
2409
2410
2418
2419
2421
2422
2432
2433
2513
2514
2515
Lot Numbers:
2407
2408
2419
2425
2429
2430
2442
2443
2444
2445
2446
2449
2450
2502
2513
2515
2516
UDI:
10381780486978
10381780486886

Indicated for light to moderately exuding wounds.

Product: MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY
Model / REF:
31012
31022
31045
Lot Numbers (127):
A24008
A24057
B21123
B24075
C22159
C23177
C24148
D24190
E21365
E24254
E24255
G23393
H21523
H22452
H23443
I22512
I23464
J21693
L22706
A23045
A23065
A25028
A25056
B23079
B25068
B25077
C21151
C21152
C21155
C21195
C22182
C22196
C23183
C23193
C25152
D23196
D23208
E21300
E22305
E22319
F21407
F21428
F21430
F22333
F24317
G23405
H21544
H22438
H23415
H23442
UDI:
10381780486909
10381780486916
10381780486923

Indicated for moderately to heavily exuding wounds.

Product: Private Label CVS (MediHoney)
Model / REF:
CVS405406
Lot Numbers:
2428
2446
2509
2514
UDI:
00050428452547

Intended for minor scalds, burns, cuts, lacerations, and abrasions.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98175
Status: Active
Manufacturer: Integra LifeSciences Corp. (NeuroSciences)
Sold By: CVS; authorized distributors; healthcare facilities
Manufactured In: United States
Units Affected: 3 products (49,367 units; 55,276 units; 2,906 units)
Distributed To: Texas, Michigan, Florida, Indiana, Missouri, California, Virginia, New Jersey, Pennsylvania, South Carolina, Tennessee, Rhode Island, New York

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.