--- title: "Integra LifeSciences Corp. (NeuroSciences) Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Integra LifeSciences Corp. (NeuroSciences) recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/integra-lifesciences-corp-neurosciences/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Integra LifeSciences Corp. (NeuroSciences) recall records **31** reported ongoing 31 records in this archive. Latest source date Jun 5, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Jun 5, 2026 FDA device enforcement ### [OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.](https://isitonrecall.com/recall/fda-device-z-2714-2026-omnitract-surgical-retractor-system-which-includes-633-of-the-firm-s-product-codes/) The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the sterilization cycle exposure time used. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Azerbaijan, Bangladesh, Belgium, Brunei Darussalam, Bulgaria, Canada, Chile, China, Czechia, Denm... [Official source for OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2714-2026%22) Apr 10, 2026 FDA device enforcement ### [Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Catheter is a 3.3 mm diameter (10 Fr.), 35 cm long polyurethan...](https://isitonrecall.com/recall/fda-device-z-2173-2026-codman-cerebroflo-evd-catheter-with-endexo-technology-contains-5-sets-product-id-37-550-501-the-cere/) Out-of-specification endotoxin result that did not meet the acceptance criteria. Class II Reported ongoing Distribution: US Nationwide distribution in the states of Arizona (AZ), Arkansas (AR), California (CA), Connecticut (CT), Florida (FL), Kentucky (KY), Louisiana (LA), Michigan (MI), Minnesota... [Official source for Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. T...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2173-2026%22) Mar 19, 2026 FDA device enforcement ### [Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.](https://isitonrecall.com/recall/fda-device-z-1816-2026-cytal-wound-matrix-2-layer-5x5-cm-product-id-wsm0505/) Increased rate of out-of-specification endotoxin results. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, AZ, CA, DC, FL, GA, IA, IL, KS, KY, LA, MD, ME, MN, MO, MT, NC, ND, NE, NJ, NY, OH, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV. [Official source for Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1816-2026%22) Mar 19, 2026 FDA device enforcement ### [Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.](https://isitonrecall.com/recall/fda-device-z-1817-2026-cytal-wound-matrix-2-layer-7x10-cm-product-id-wsm0710/) Increased rate of out-of-specification endotoxin results. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, AZ, CA, DC, FL, GA, IA, IL, KS, KY, LA, MD, ME, MN, MO, MT, NC, ND, NE, NJ, NY, OH, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV. [Official source for Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1817-2026%22) Mar 19, 2026 FDA device enforcement ### [Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.](https://isitonrecall.com/recall/fda-device-z-1818-2026-cytal-wound-matrix-2-layer-10x15-cm-product-id-wsm1015/) Increased rate of out-of-specification endotoxin results. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, AZ, CA, DC, FL, GA, IA, IL, KS, KY, LA, MD, ME, MN, MO, MT, NC, ND, NE, NJ, NY, OH, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV. [Official source for Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1818-2026%22) Mar 19, 2026 FDA device enforcement ### [Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.](https://isitonrecall.com/recall/fda-device-z-1819-2026-cytal-burn-matrix-7x10-cm-product-id-bmm0710/) Increased rate of out-of-specification endotoxin results. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, AZ, CA, DC, FL, GA, IA, IL, KS, KY, LA, MD, ME, MN, MO, MT, NC, ND, NE, NJ, NY, OH, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV. [Official source for Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1819-2026%22) Mar 19, 2026 FDA device enforcement ### [Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.](https://isitonrecall.com/recall/fda-device-z-1820-2026-cytal-burn-matrix-10x15-cm-product-id-bmm1015/) Increased rate of out-of-specification endotoxin results. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, AZ, CA, DC, FL, GA, IA, IL, KS, KY, LA, MD, ME, MN, MO, MT, NC, ND, NE, NJ, NY, OH, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV. [Official source for Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1820-2026%22) Mar 6, 2026 FDA device enforcement ### [CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.](https://isitonrecall.com/recall/fda-device-z-1828-2026-cusa-clarity-c7000-console-software-version-2-1-1-909-ultrasonic-surgical-aspirator-system/) Software issue that renders the touch screen unresponsive. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of MI & NY. The countries of Belgium, China, Czechia, Dubai, Finland, France, Germany, Italy, Japan, Luxembourg, Netherlands... [Official source for CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1828-2026%22) Jan 16, 2026 FDA device enforcement ### [MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with Active Leptospermum Honey provides a moist environment con...](https://isitonrecall.com/recall/fda-device-z-1363-2026-medihoney-gel-with-active-leptospermum-honey-model-catalog-numbers-1-31805-2-31815-medihoney-gel-dre/) Potential packaging failures, which could lead to a breach in the sterile barrier. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of TX, MI, FL, IN, MO, CA, VA, NJ, PA, SC, TN, RI, NY and the countries of Australia, Austria, Bahrain, Canada, Finland, Fra... [Official source for MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1363-2026%22) Jan 16, 2026 FDA device enforcement ### [MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers: (1) 31012, (2) 31022, (3) 31045. MEDIHONEY CALCIUM ALGINATE DRESSING WITH ACTIVE LEPTOSPERMUM HONEY sup...](https://isitonrecall.com/recall/fda-device-z-1364-2026-medihoney-calcium-alginate-with-active-leptospermum-honey-model-numbers-1-31012-2-31022-3-31045-medi/) Potential packaging failures, which could lead to a breach in the sterile barrier. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of TX, MI, FL, IN, MO, CA, VA, NJ, PA, SC, TN, RI, NY and the countries of Australia, Austria, Bahrain, Canada, Finland, Fra... [Official source for MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers: (1) 31012, (2) 31022, (...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1364-2026%22) Jan 16, 2026 FDA device enforcement ### [Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment, which has shown to be conducive to wound healing. Intended for minor scalds & burns, minor ...](https://isitonrecall.com/recall/fda-device-z-1365-2026-private-label-cvs-model-number-cvs405406-helps-maintain-a-moist-wound-environment-which-has-shown-to/) Potential packaging failures, which could lead to a breach in the sterile barrier. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of TX, MI, FL, IN, MO, CA, VA, NJ, PA, SC, TN, RI, NY and the countries of Australia, Austria, Bahrain, Canada, Finland, Fra... [Official source for Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment, which has s...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1365-2026%22) Dec 12, 2025 FDA device enforcement ### [Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is required. The kit is indicated for use...](https://isitonrecall.com/recall/fda-device-z-1036-2026-codman-microsensor-basic-kit-catalog-number-626631us-use-of-the-codman-microsensor-basic-kit-is-indi/) Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, N... [Official source for Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit i...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1036-2026%22) Dec 12, 2025 FDA device enforcement ### [Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Codman CereLink ICP Sensor Basic Kit consists of the CereLink ICP Sensor (ICP Sensor) and a 14-gauge Tuohy need...](https://isitonrecall.com/recall/fda-device-z-1037-2026-codman-cerelink-icp-sensor-basic-kit-catalog-number-826850-the-codman-cerelink-icp-sensor-basic-kit/) Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, N... [Official source for Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Codman CereLink ICP Sensor Basi...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1037-2026%22) Oct 3, 2025 FDA device enforcement ### [TruDi¿ Navigation System - Multi Instrument Adapter; - Manufacturer's Product Number (Catalog Number): EM-2025-000F Rev 00 or Rev 01;](https://isitonrecall.com/recall/fda-device-z-0420-2026-trudi-navigation-system-multi-instrument-adapter-manufacturer-s-product-number-catalog-number-em-202/) It was determined that when the navigation system is configured with specific revision combinations of the Multi Instrument Adapter together with the Patient Tracker the system may not meet its specified accuracy for visual verification of device location w... Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for TruDi¿ Navigation System - Multi Instrument Adapter; - Manufacturer's Product Number (Catalog Num...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0420-2026%22) Sep 26, 2025 FDA device enforcement ### [CODMAN Disposable Perforator 11mm. Cranial Perforator.](https://isitonrecall.com/recall/fda-device-z-0373-2026-codman-disposable-perforator-11mm-cranial-perforator/) Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution. Class I Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Bahamas, Barbados, Belgium, Brazil, Canada, Chile, Colombia, Cyprus, Czechia, Ecuador,... [Official source for CODMAN Disposable Perforator 11mm. Cranial Perforator.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0373-2026%22) Sep 26, 2025 FDA device enforcement ### [CODMAN Disposable Perforator 9mm. Cranial Perforator.](https://isitonrecall.com/recall/fda-device-z-0374-2026-codman-disposable-perforator-9mm-cranial-perforator/) Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution. Class I Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Bahamas, Barbados, Belgium, Brazil, Canada, Chile, Colombia, Cyprus, Czechia, Ecuador,... [Official source for CODMAN Disposable Perforator 9mm. Cranial Perforator.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0374-2026%22) Aug 5, 2025 FDA device enforcement ### [Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿ Paste with Active Leptospermum Honey is a moist dressing made ...](https://isitonrecall.com/recall/fda-device-z-2505-2025-brand-name-medihoney-product-name-medihoney-paste-model-catalog-number-31505-product-description-med/) Packaging failures were identified which could lead to a breach in the sterile barrier. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE,... [Official source for Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Descri...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2505-2025%22) Aug 5, 2025 FDA device enforcement ### [Brand Name: MediHoney ¿ Product Name: MediHoney ¿ Tube Model/Catalog Number: 31515 and 31535 Product Description: MediHoney¿ Paste with Active Leptospermum Honey is a moist dres...](https://isitonrecall.com/recall/fda-device-z-2506-2025-brand-name-medihoney-product-name-medihoney-tube-model-catalog-number-31515-and-31535-product-descri/) Packaging failures were identified which could lead to a breach in the sterile barrier. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE,... [Official source for Brand Name: MediHoney ¿ Product Name: MediHoney ¿ Tube Model/Catalog Number: 31515 and 31535 Prod...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2506-2025%22) Aug 5, 2025 FDA device enforcement ### [Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Sheet Dressing with Leptospermum Model/Catalog Number: 31612, 31622, 31644 Product Description: MEDIHONEY¿ HCS SHEET DRESSING...](https://isitonrecall.com/recall/fda-device-z-2507-2025-brand-name-medihoney-product-name-medihoney-hcs-sheet-dressing-with-leptospermum-model-catalog-numbe/) Packaging failures were identified which could lead to a breach in the sterile barrier. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE,... [Official source for Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Sheet Dressing with Leptospermum Model/Catalo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2507-2025%22) Aug 5, 2025 FDA device enforcement ### [Brand Name: MediHoney¿ Product Name: MediHoney¿ Adhesive Hydrogel Sheet Dressing Model/Catalog Number: 31720, 31740 Product Description: MEDIHONEY¿ Adhesive Hydrogel Sheet Dress...](https://isitonrecall.com/recall/fda-device-z-2508-2025-brand-name-medihoney-product-name-medihoney-adhesive-hydrogel-sheet-dressing-model-catalog-number-31/) Packaging failures were identified which could lead to a breach in the sterile barrier. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE,... [Official source for Brand Name: MediHoney¿ Product Name: MediHoney¿ Adhesive Hydrogel Sheet Dressing Model/Catalog Nu...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2508-2025%22) ## Reasons in these listed records - The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the sterilization cycle exposure time used. - Out-of-specification endotoxin result that did not meet the acceptance criteria. - Increased rate of out-of-specification endotoxin results. - Software issue that renders the touch screen unresponsive. These examples come from this result page and are not a ranking of every recall reason. ## Checking Integra LifeSciences Corp. (NeuroSciences) ### Is there a recall on integra lifesciences corp. (neurosciences) right now? This archive contains 31 records, including 31 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Integra LifeSciences Corp. (NeuroSciences)](https://isitonrecall.com/check/?q=Integra%20LifeSciences%20Corp.%20%28NeuroSciences%29) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)