International safety notice

72201992|72201996|72202165

New Zealand / Medsafe Recalls · NZL · Aug 12, 2013

Key facts

Title 72201992|72201996|72202165
Regulator New Zealand / Medsafe Recalls
Country NZL
Brand Smith & Nephew OsteoraptorSuture Anchor with Ultrabraid Suture
Manufacturer Smith & Nephew Inc
Models 72201992, 72201996, 72202165
Event type Recall
Action type Recall
Date Aug 12, 2013
Regulator page medsafe.govt.nz

At a glance

  • Yes Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices