Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Integra HRAIM Head Ring Assembly with Intubation Mounts The CRW Recalled by Integra LifeSciences Corporation Due to T-handle screw is used on a complementary product...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Integra LifeSciences Corporation directly.
Affected Products
Integra HRAIM Head Ring Assembly with Intubation Mounts The CRW stereotactic system is used in conjunction with the HRAIM head ring is a target-centered system that can be configured to be CT-only or CT/MR compatible. The CRW stereotactic system is a multi-purpose system used for localizing intercranial targets for precisely directing instruments such as: Biopsy forceps RF lesioning electrodes Deep brain electrodes Recording and stimulating electrodes
Quantity: 188 units
Why Was This Recalled?
T-handle screw is used on a complementary product to the CRW, the Integra HRAIM, which is the CT-compatible intubation Head Ring Assembly. When the T-handle on the HRAIM intubation hoop is tightened, the T-handle could stop in a vertical position that prevents the CRWPRECISE and certain models of the CRW-ASL from seating properly on the head ring although it appears to be fully seated
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Integra LifeSciences Corporation
Integra LifeSciences Corporation has 29 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report