International safety notice

Urgent field safety notice for Solus Flexible - small paediatric, wire-reinforced laryngeal mask airway 2 / large paediatric, wire-reinforced laryngeal mask airway 2.5 / small adult, wire-reinforced laryngeal mask airway 3 / medium adult, wire-reinforced laryngeal mask airway 4 / large adult, wire-reinforced laryngeal mask airway 5, Intersurgical Ltd.

Germany / BfArM · DEU · Mar 30, 2017

Key facts

Title Urgent field safety notice for Solus Flexible - small paediatric, wire-reinforced laryngeal mask airway 2 / large paediatric, wire-reinforced laryngeal mask airway 2.5 / small adult, wire-reinforced laryngeal mask airway 3 / medium adult, wire-reinforced laryngeal mask airway 4 / large adult, wire-reinforced laryngeal mask airway 5, Intersurgical Ltd.
Regulator Germany / BfArM
Country DEU
Brand Solus Flexible - small paediatric, wire-reinforced laryngeal mask airway 2 / large paediatric, wire-reinforced laryngeal mask airway 2.5 / small adult, wire-reinforced laryngeal mask airway 3 / medium adult, wire-reinforced laryngeal mask airway 4 / large adult, wire-reinforced laryngeal mask airway 5, Intersurgical Ltd.
Manufacturer Urgent field safety notice for Solus Flexible - small paediatric, wire-reinforced laryngeal mask airway 2 / large paediatric, wire-reinforced laryngeal mask airway 2.5 / small adult, wire-reinforced laryngeal mask airway 3 / medium adult, wire-reinforced laryngeal mask airway 4 / large adult, wire-reinforced laryngeal mask airway 5, Intersurgical Ltd.
Models 8003001, 8025001, 8005001, 8002001, 31703855, 31310139, 164826, 8004001
Date Mar 30, 2017
Regulator page bfarm.de

At a glance

  • No 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