Integra LifeSciences (NeuroSciences) recalls

3 recent recalls on record for Integra LifeSciences (NeuroSciences) in CPSC, NHTSA, and FDA data as of July 24, 2026 at 12:00 AM UTC.

Models with recalls

CUSA Clarity C7000 Console (1)Codman CerebroFlo EVD Catheter with Endexo Technology (1)OmniTract Surgical Retractor System (1)

All Integra LifeSciences (NeuroSciences) recalls

FDA Class II · Medical device · July 15, 2026

OmniTract Surgical Retractor System recall — Integra LifeSciences Corp. (NeuroSciences)

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 …

Official ID Z-2714-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Codman CerebroFlo EVD Catheter with Endexo Technology recall — Integra LifeSciences Corp. (NeuroSciences)

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

Official ID Z-2173-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

CUSA Clarity C7000 Console recall — Integra LifeSciences Corp. (NeuroSciences)

Software issue that renders the touch screen unresponsive.

Official ID Z-1828-2026 · Official record ↗

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (vehicles aggregated here; car seats & tires not yet)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & egg products ↗ (not yet aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from official public-domain government data. Last checked July 24, 2026 at 12:00 AM UTC.