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Recall 52113 — Trident Acetabular System Hemispherical Surgical Protocol and Trident Product Reference Guide (2014-09-22)

Health Canada Consumer Product Safety · Canada · 2014-10-09 · Type II

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Agency: Health Canada Consumer Product Safety
Recall identifier: 52113
Date of alert: 2014-10-09
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Medical devices
Product type: Medical devices

Reported risk: Medical devices

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/trident-acetabular-system-hemi

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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.

Recall 52113 — Trident Acetabular System Hemispherical Surgical Protocol and Trident Product Reference Guide (2014-09-22)

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