International safety notice

Safety Notice concerning several models of SlingBars, Liko GmbH

Germany / BfArM · DEU · Nov 22, 2013

Key facts

Title Safety Notice concerning several models of SlingBars, Liko GmbH
Regulator Germany / BfArM
Country DEU
Brand Safety Notice concerning several models of SlingBars, Liko GmbH
Manufacturer Safety Notice concerning several models of SlingBars, Liko GmbH
Models 180849, 3156084, 3156012, 3156011, 3156008, 800774, 3153012, 3156094, 3156015, 3156087, 3156017, 800509 and 10 more
Date Nov 22, 2013
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 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

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