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

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.

© 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Surgical Equipment

Integra LifeSciences Corp.: Codman Surgical Patties and Strips Recalled for High Endotoxin Levels

Agency Publication Date: October 29, 2024
Share:
Sign in to monitor this recall

Summary

Approximately 817,695 units of Codman Surgical Patties and Codman Surgical Strips have been recalled by Integra LifeSciences Corp. because higher-than-expected levels of endotoxins were found in the raw materials used to make them. Endotoxins are substances from bacteria that can cause serious inflammatory reactions when they enter the body. These products are cotton-based materials used to protect delicate tissue, including the brain and central nervous system, during surgery. All unexpired products distributed worldwide and nationwide in the U.S. are affected.

Risk

Elevated levels of endotoxins in surgical materials can cause severe inflammation, fever, or other systemic reactions in patients, which is particularly dangerous when these materials are used on sensitive tissues like the brain or spinal cord during surgery.

What You Should Do

  1. Check your surgical inventory for CODMAN Surgical Patties or CODMAN Surgical Strips marked with the following catalog numbers: 801396, 801397, 801398, 801399, 801400, 801401, 801402, 801403, 801404, 801406, 801407, 801408, 801409, 801449, 801450, 801451, 801452, 801453, 801454, 801455, 801456, or 801457.
  2. Examine the product packaging for UDI numbers. Note that due to a company transition, products may be labeled under either 'JnJ' (Johnson & Johnson) or 'Integra' identifiers. All unexpired lots of these products are included in this recall.
  3. Immediately stop using any affected surgical patties or strips and quarantine them to prevent clinical use.
  4. Contact your healthcare provider if you have concerns about procedures where these materials may have been used.
  5. Contact Integra LifeSciences Corp. at their Princeton, NJ headquarters or through their official website to arrange for the return of affected inventory and to discuss potential remedies.
  6. For additional questions or to report adverse events, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

📋Other Action

Quarantine and return product inventory

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: MICR PATIE RND
Model / REF:
801396
Lot Numbers:
UDI# 10381780514923
UDI# 20886704036446
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1/4X1-1/2
Model / REF:
801397
Lot Numbers:
UDI# 10381780514930
UDI# 20886704036453
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1/4X3
Model / REF:
801398
Lot Numbers:
UDI# 10381780514947
UDI# 20886704036460
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1/4X1/4
Model / REF:
801399
Lot Numbers:
UDI# 10381780514954
UDI# 20886704036477
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1/2X1/2
Model / REF:
801400
Lot Numbers:
UDI# 10381780514961
UDI# 20886704036484
Date Ranges: All unexpired products
Product: SURG PAT XRAY 3/4X3/4
Model / REF:
801401
Lot Numbers:
UDI# 10381780514978
UDI# 20886704036491
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1/2X1
Model / REF:
801402
Lot Numbers:
UDI# 10381780514985
UDI# 20886704036507
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1X1
Model / REF:
801403
Lot Numbers:
UDI# 10381780514992
UDI# 20886704036514
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1/2X1-1/2
Model / REF:
801404
Lot Numbers:
UDI# 10381780515005
UDI# 20886704036521
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1/2X2
Model / REF:
801406
Lot Numbers:
UDI# 10381780515012
UDI# 20886704036538
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1/2X3
Model / REF:
801407
Lot Numbers:
UDI# 10381780515029
UDI# 20886704036545
Date Ranges: All unexpired products
Product: SURG PAT XRAY 1X3
Model / REF:
801408
Lot Numbers:
UDI# 10381780515036
UDI# 20886704036552
Date Ranges: All unexpired products
Product: SURG PAT XRAY 3X3
Model / REF:
801409
Lot Numbers:
UDI# 10381780515043
UDI# 20886704036569
Date Ranges: All unexpired products
Product: SURG STRP 1/8X6
Model / REF:
801449
Lot Numbers:
UDI# 10381780515050
UDI# 20886704036576
Date Ranges: All unexpired products
Product: SURG STRP 1/4X6
Model / REF:
801450
Lot Numbers:
UDI# 10381780515067
UDI# 20886704036583
Date Ranges: All unexpired products
Product: SURG STRP 1/2X6
Model / REF:
801451
Lot Numbers:
UDI# 10381780515074
UDI# 20886704036590
Date Ranges: All unexpired products
Product: SURG STRP 3/4X6
Model / REF:
801452
Lot Numbers:
UDI# 10381780515081
UDI# 20886704036606
Date Ranges: All unexpired products
Product: SURG STRP 1X6-200
Model / REF:
801453
Lot Numbers:
UDI# 10381780515098
UDI# 20886704036613
Date Ranges: All unexpired products
Product: SURG STRP 1-1/2X6
Model / REF:
801454
Lot Numbers:
UDI# 10381780515104
UDI# 20886704036620
Date Ranges: All unexpired products
Product: SURG STRP 2X6
Model / REF:
801455
Lot Numbers:
UDI# 10381780515111
UDI# 20886704036637
Date Ranges: All unexpired products
Product: SURG STRP 3X6
Model / REF:
801456
Lot Numbers:
UDI# 10381780515128
UDI# 20886704036644
Date Ranges: All unexpired products
Product: SURG STRP 3-1/2X6
Model / REF:
801457
Lot Numbers:
UDI# 10381780515135
UDI# 20886704036651
Date Ranges: All unexpired products

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95432
Status: Active
Manufacturer: Integra LifeSciences Corp.
Sold By: authorized medical distributors; hospitals; surgical centers
Manufactured In: United States
Units Affected: 21 products (1791; 2615; 2894; 21553; 168803; 33478; 80515; 44231; 69179; 56082; 201914; 93782; 9563; 826; 6706; 4818; 10719; 2056; 1222; 1454 units; 3494 units)
Distributed To: Nationwide

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 · 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.