Integra LifeSciences Corp. (NeuroSciences) recalls

13 recalls in our records from 2025 to 2026: 13 FDA medical devices.

Recalls with full detail pages

• FDA · Medical devicesClass INov 12, 2025

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: 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.

• FDA · Medical devicesClass IJul 2, 2025

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: MicroMyst Applicator

  Lack of sterility assurance.

• FDA · Medical devicesClass IJul 2, 2025

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: Extended Tip Applicator

  Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.

• FDA · Medical devicesClass IMay 14, 2025

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: CODMAN Disposable Perforator

  Inadequate weld that can potentially cause the product to disassemble.

Earlier and other recalls

These link to the official agency notice.

• FDA · Medical devicesClass IIJul 15, 2026

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: OmniTract Surgical Retractor System Official notice ↗

  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…

• FDA · Medical devicesClass IIMay 20, 2026

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5… Official notice ↗

  Out-of-specification endotoxin result that did not meet the acceptance criteria.

• FDA · Medical devicesClass IIApr 29, 2026

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: CUSA Clarity C7000 Console Official notice ↗

  Software issue that renders the touch screen unresponsive.

• FDA · Medical devicesClass IIApr 22, 2026

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505 Official notice ↗

  Increased rate of out-of-specification endotoxin results.

• FDA · Medical devicesClass IIFeb 25, 2026

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers Official notice ↗

  Potential packaging failures, which could lead to a breach in the sterile barrier.

• FDA · Medical devicesClass IIJan 14, 2026

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the… Official notice ↗

  Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.

• FDA · Medical devicesClass IINov 12, 2025

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: TruDi¿ Navigation System - Multi Instrument Adapter Official notice ↗

  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…

• FDA · Medical devicesClass IISep 10, 2025

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog… Official notice ↗

  Packaging failures were identified which could lead to a breach in the sterile barrier.

• FDA · Medical devicesClass IIMay 14, 2025

  Integra LifeSciences Corp. (NeuroSciences) medical device recall: INSPIRA AIR BALLOON DILATION SYSTEM 10x40 Official notice ↗

  Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.

Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.