Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2227-2017 — 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

U.S. FDA — Device Enforcement · Canada · 2008-06-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2227-2017
Date of alert: 2008-06-04
Country / jurisdiction: Canada
Risk level: Class II
Risk type: recall
Brand: Orthosoft, Inc. dba Zimmer CAS
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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