Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sesamoid Plasty Recalled by Orthosoft, Inc. dba Zimmer CAS Due to Zimmer CAS voluntarily conducted a retrospective recall of...
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 Orthosoft, Inc. dba Zimmer CAS directly.
Affected Products
Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Plasty workstation is used to run the tracking software as part of the software based navigation systems. The affected Sesamoid Plasty components are the central structural column and its base that hold up the computer and the tracking camera on the Sesamoid Plasty workstation. They are also designed to be disassembled such that the column can be folded onto itself for ease of transport after use. This is a retrospective recall report for a removal initiated on 17 June 2008
Quantity: 10
Why Was This Recalled?
Zimmer CAS voluntarily conducted a retrospective recall of the Sesamoid Plasty due to the risk of the top of the workstation to potentially fall over during disassembly.
Where Was This Sold?
This product was distributed to 2 states: CA, FL
About Orthosoft, Inc. dba Zimmer CAS
Orthosoft, Inc. dba Zimmer CAS has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report