Product Wiki · Recalls · Health Canada — Medical Devices

Da Vinci S and Da Vinci SI Surgical Systems (2013-07-22) — recall 50260

Health Canada — Medical Devices · Canada · 2013-12-04 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 50260
Date of alert: 2013-12-04
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: Voluntary action to provide users with additional information regarding sterile adapter engagement and instrument installation. Although rare, sterile adapter and instrument engagement issues may lead to non-intuitive motion or a sluggish response when controlling instruments. These characteristics are apparent prior to interaction with tissue and thus do not pose a risk to health or safety of patients or users.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/da-vinci-s-and-da-vinci-si-sur

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.

Da Vinci S and Da Vinci SI Surgical Systems (2013-07-22) — recall 50260

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