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Recall Observatory FDA recall evidence

Device product

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

Z-2227-2017

June 04, 2008

Class II

Product summary

Firm
Orthosoft, Inc. dba Zimmer CAS
Event
Event 75609
Status
Terminated
Classification
Class II
Quantity
10
Official record key
device-enforcement:Z-2227-2017

Official wording

Reason: 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.

Code information: Part Number and : 521.025/521.028; Lot Number/Serial Numbers: SP-001, SP-002, SP-003, SP-004, SP-005, SP-006, SP-007, SP-008, SP-009, SP-010

Distribution pattern: Worldwide Distribution - US including FL, CA Foreign: Austrailia, New Zealand, France, Brazil

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.