Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PSI Knee System- Prosthesis Recalled by Zimmer CAS Due to Internal discovery found that the MRI scans in...
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 Zimmer CAS directly.
Affected Products
PSI Knee System- Prosthesis, knee patellofemorotibial, semi-constrained, cemented, polymer/meal/polymer The Zimmer PSI Knee System is indicated as an orthopedic instrument system to assist in the positioning of knee replacement components.
Quantity: 15
Why Was This Recalled?
Internal discovery found that the MRI scans in some PSI knee guides involved an additional rotation adjustments that could potentially lead to misalignment due to a design flaw.
Where Was This Sold?
This product was distributed to 5 states: AZ, CO, IL, OR, WA
About Zimmer CAS
Zimmer CAS has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report