Integra LifeSciences Corp. (NeuroSciences) recalls
Every recall we track for Integra LifeSciences Corp. (NeuroSciences) — 31 in all, from 2025–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Integra LifeSciences Corp. (NeuroSciences) peaked in 2025 (20); 31 since 2017.
All FDA recall records for Integra LifeSciences Corp. (NeuroSciences) since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 1 | 19 | 0 | 20 |
| 2026 (to date) | 0 | 0 | 10 | 1 | 11 |
Most common reasons for Integra LifeSciences Corp. (NeuroSciences) recalls
What to do if you have a recalled Integra LifeSciences Corp. (NeuroSciences) product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Integra LifeSciences Corp. (NeuroSciences) recalls
13 shown- Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
Integra LifeSciences recalls 633 OmniTract Surgical Retractor System models due to dry time not being extended to 90-120 minutes as required for sterilization cycles.
Integra LifeSciencesJun 5, 2026 - UnratedMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD
Integra LifeSciences recalls Codman CerebroFlo EVD catheters with endotoxin results outside safety limits. Affected units have Product ID 37.550.501. Contact for remedy details.
Integra LifeSciencesApr 10, 2026 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.
Integra LifeSciences recalls Cytal Burn Matrix 10x15 cm products with endotoxin out-of-specification results. Affected units include specific lot numbers and product IDs. Consumers should contact Integra for details.
Integra LifeSciencesMar 19, 2026 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.
Integra LifeSciences recalls C7000 Console software version 2.1.1.909 due to touch screen unresponsiveness. Affected units have specific serial numbers and model.
Integra NeuroSciencesMar 6, 2026 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with
Integra LifeSciences recalls MediHoney Gel dressings with model numbers 31805 and 31815 due to potential packaging failures that could breach the sterile barrier. Affected units include specific serial and lot numbers.
Integra LifeSciencesJan 16, 2026 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when
Integra NeuroSciences recalls Codman Microsensor Basic Kit (Catalog 626631US) due to potential corrosion stains on the 14-gauge Tuohy Needle. This may affect subdural and intraparenchymal pressure monitoring.
Integra NeuroSciencesDec 12, 2025 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls TruDi¿ Navigation System - Multi Instrument Adapter; - Manufacturer's Product Number (Catalog Number): EM-2025-000F Rev
Integra LifeSciences recalls TruDi Navigation System Multi Instrument Adapters (EM-2025-000F Rev 00/01) due to potential accuracy problems during patient anatomy verification. Affected users should contact for details.
Integra LifeSciencesOct 3, 2025 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls CODMAN Disposable Perforator 11mm. Cranial Perforator.
Integra NeuroSciences recalls CODMAN Disposable Perforators 11mm and 9mm models with inadequate welds. Affected units have specific lot numbers and expiration dates. Consumers should check their product details.
Integra NeuroSciencesSep 26, 2025 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿
Integra LifeSciences recalls MediHoney Paste 31505 due to potential sterile packaging breaches. This could compromise wound healing. Affected units include specific lot numbers.
MediHoneyAug 5, 2025 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with the Integra Flow
Integra LifeSciences recalls MicroMyst Applicators due to lack of sterility assurance. Affected units include all lots of model 20500:500DS. Consumers should contact Integra for details.
IntegraMay 23, 2025 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls Extended Tip Applicator, 15 CM, Box of 5.
Integra LifeSciences recalls 15cm Extended Tip Applicators (box of 5) due to potential endotoxin levels and lack of sterility. Affected units include all lots with model 205115.
Integra LifeSciencesMay 22, 2025 - Use cautionMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls CODMAN Craniotomy Kit, Disposable Perforator Cranio-blade Wire Pass Drill, 14mm. Cranial perforator kit.
Integra LifeSciences recalls disposable cranial perforator kits with a potential weld issue that could cause disassembly. Affected models include specific lot numbers and UDI codes.
Integra NeuroSciencesApr 11, 2025 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.
Integra LifeSciences recalls INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK due to incorrect product packaging in carton. Affected units include specific model and lot numbers.
Integra LifeSciencesApr 4, 2025
Integra LifeSciences Corp. (NeuroSciences) recall questions
How many recalls has Integra LifeSciences Corp. (NeuroSciences) had?
31 recalls from Integra LifeSciences Corp. (NeuroSciences) are on record with U.S. safety agencies, from 2025–2026.
What is the most recent Integra LifeSciences Corp. (NeuroSciences) recall?
Integra LifeSciences Corp. (NeuroSciences) recalls OmniTract Surgical Retractor System, which includes 633 of the firm s product codes., dated Jun 5, 2026. Every Integra LifeSciences Corp. (NeuroSciences) recall is listed on this page, newest first.
Why are Integra LifeSciences Corp. (NeuroSciences) products recalled?
The most common reasons on record: Increased rate of out-of-specification endotoxin results. (5); Inadequate weld that can potentially cause the product to disassemble. (2).
What should I do if I have a recalled Integra LifeSciences Corp. (NeuroSciences) product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Integra LifeSciences Corp. (NeuroSciences) recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.