Orthosoft, Inc. dba Zimmer CAS: Medical Device Recall in 2017 - (Recall #: Z-2227-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 4, 2008

Date Posted: June 14, 2017

Recall Number: Z-2227-2017

Event ID: 75609

Reason for Recall:

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.

Status: Terminated

Product Quantity: 10

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

Voluntary or Mandated:

Voluntary: Firm initiated