Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT Recalled by Integra LifeSciences Corp. Due to There is a potential for the knob assembly...
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 Corp. directly.
Affected Products
MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT, Part Number A2079A The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp is necessary, positional freedom is required and where X-ray imaging modalities will be used.
Quantity: 1 units
Why Was This Recalled?
There is a potential for the knob assembly in the swivel adapter to fracture/break during use.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Integra LifeSciences Corp.
Integra LifeSciences Corp. has 216 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report