International safety notice

• Pala de laringoscopio de un solo uso Rusch® Greenlite™ (MAC 3) Referencia 004551003 • Pala de laringoscopio de un solo uso Rusch® Greenlite™ (MAC 4) Referencia 004551004

Spain / AEMPS · ESP · Jan 30, 2020

Key facts

Title • Pala de laringoscopio de un solo uso Rusch® Greenlite™ (MAC 3) Referencia 004551003 • Pala de laringoscopio de un solo uso Rusch® Greenlite™ (MAC 4) Referencia 004551004
Regulator Spain / AEMPS
Country ESP
Brand • Pala de laringoscopio de un solo uso Rusch® Greenlite™ (MAC 3) Referencia 004551003 • Pala de laringoscopio de un solo uso Rusch® Greenlite™ (MAC 4) Referencia 004551004
Manufacturer Teleflex Medical, Irlanda.
Models 1902331, 1811331, 004551004, 1904331, 004551003, 1812341, 28022, 91.822.52.89, 004551003PALA, 649392681, EIF-000393, 57161 and 4 more
Event type Safety Notice
Date Jan 30, 2020

At a glance

  • No Recall
  • Yes 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